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    "count": 217334,
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    "results": [
        {
            "created": "2016-11-29T15:56:11.559000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed SLC6A3",
            "entity_name": "SLC6A3",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:52:24.267000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed PLA2G6",
            "entity_name": "PLA2G6",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:41:59.414000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed PINK1",
            "entity_name": "PINK1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:39:20.485000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed PARK7",
            "entity_name": "PARK7",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:33:44.143000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed PARK2",
            "entity_name": "PARK2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:30:28.798000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed PANK2",
            "entity_name": "PANK2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:26:25.008000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed MAPT",
            "entity_name": "MAPT",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:24:02.988000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed MAPT",
            "entity_name": "MAPT",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:11:14.961000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed GCH1",
            "entity_name": "GCH1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:07:49.879000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed FTL",
            "entity_name": "FTL",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T15:01:58.842000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed FBXO7",
            "entity_name": "FBXO7",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T14:58:20.379000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed DCTN1",
            "entity_name": "DCTN1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T14:55:05.113000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed C19orf12",
            "entity_name": "C19orf12",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T14:37:53.818000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Arianna Tucci",
            "item_type": "entity",
            "text": "reviewed ATP13A2",
            "entity_name": "ATP13A2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:23:03.840000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked IFIH1 as ready",
            "entity_name": "IFIH1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:21:11.124000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified IFIH1 as green",
            "entity_name": "IFIH1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:12:27.553000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ERCC6 as amber",
            "entity_name": "ERCC6",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:12:27.552000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on ERCC6",
            "entity_name": "ERCC6",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:05:44.325000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CYP2U1 as amber",
            "entity_name": "CYP2U1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:02:28.072000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CYP2U1 as red",
            "entity_name": "CYP2U1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:02:28.071000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on CYP2U1",
            "entity_name": "CYP2U1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:00:32.970000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CTC1 as green",
            "entity_name": "CTC1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T13:00:09.213000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked CTC1 as ready",
            "entity_name": "CTC1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T12:54:03.619000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CTC1 as red",
            "entity_name": "CTC1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T12:54:03.617000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on CTC1",
            "entity_name": "CTC1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T12:42:32.953000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked COL4A1 as ready",
            "entity_name": "COL4A1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T12:41:07.770000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified COL4A1 as green",
            "entity_name": "COL4A1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T12:33:18.237000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified COL4A1 as amber",
            "entity_name": "COL4A1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T12:33:18.236000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on COL4A1",
            "entity_name": "COL4A1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T12:02:47.519000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified AP1S2 as amber",
            "entity_name": "AP1S2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T12:02:47.519000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on AP1S2",
            "entity_name": "AP1S2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:47:43.412000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked ADAR as ready",
            "entity_name": "ADAR",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:44:58.567000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ADAR as green",
            "entity_name": "ADAR",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:42:45.643000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ADAR as red",
            "entity_name": "ADAR",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:42:45.642000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on ADAR",
            "entity_name": "ADAR",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:35:58.307000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked ACP5 as ready",
            "entity_name": "ACP5",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:32:23.985000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ACP5 as green",
            "entity_name": "ACP5",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:32:23.984000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on ACP5",
            "entity_name": "ACP5",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:26:06.300000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked TREX1 as ready",
            "entity_name": "TREX1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:25:04.787000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TREX1 as green",
            "entity_name": "TREX1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:20:45.712000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked PDGFRB as ready",
            "entity_name": "PDGFRB",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T11:19:45.170000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified PDGFRB as green",
            "entity_name": "PDGFRB",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:30:56.561000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked PDGFB as ready",
            "entity_name": "PDGFB",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:27:45.654000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified PDGFB as green",
            "entity_name": "PDGFB",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:27:45.653000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on PDGFB",
            "entity_name": "PDGFB",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:24:46.539000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified PDGFRB as amber",
            "entity_name": "PDGFRB",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:16:26.760000Z",
            "panel_name": "Sudden death in young people",
            "panel_id": 45,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "reviewed SLC6A4",
            "entity_name": "SLC6A4",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:11:49.984000Z",
            "panel_name": "Sudden death in young people",
            "panel_id": 45,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "reviewed MAOA",
            "entity_name": "MAOA",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:10:09.760000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SLC20A2 as amber",
            "entity_name": "SLC20A2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:09:19.373000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SLC20A2 as green",
            "entity_name": "SLC20A2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:09:19.372000Z",
            "panel_name": "Intracerebral calcification disorders",
            "panel_id": 315,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on SLC20A2",
            "entity_name": "SLC20A2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:09:03.284000Z",
            "panel_name": "Sudden death in young people",
            "panel_id": 45,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "reviewed KCND3",
            "entity_name": "KCND3",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:06:11.778000Z",
            "panel_name": "Sudden death in young people",
            "panel_id": 45,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "reviewed KCND2",
            "entity_name": "KCND2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:03:32.231000Z",
            "panel_name": "Sudden death in young people",
            "panel_id": 45,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "commented on CACNA2D1",
            "entity_name": "CACNA2D1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T10:00:36.918000Z",
            "panel_name": "Sudden death in young people",
            "panel_id": 45,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "commented on ACADM",
            "entity_name": "ACADM",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-29T09:56:42.483000Z",
            "panel_name": "Sudden death in young people",
            "panel_id": 45,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "reviewed PHOX2B",
            "entity_name": "PHOX2B",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T20:50:44.772000Z",
            "panel_name": "Posterior segment abnormalities",
            "panel_id": 307,
            "panel_version": null,
            "user_name": "Mervyn Thomas",
            "item_type": "entity",
            "text": "added SLC38A8 to panel",
            "entity_name": "SLC38A8",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T20:50:42.906000Z",
            "panel_name": "Posterior segment abnormalities",
            "panel_id": 307,
            "panel_version": null,
            "user_name": "Mervyn Thomas",
            "item_type": "entity",
            "text": "reviewed SLC38A8",
            "entity_name": "SLC38A8",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T20:46:59.516000Z",
            "panel_name": "Posterior segment abnormalities",
            "panel_id": 307,
            "panel_version": null,
            "user_name": "Mervyn Thomas",
            "item_type": "entity",
            "text": "reviewed GPR143",
            "entity_name": "GPR143",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T20:32:14.308000Z",
            "panel_name": "Infantile nystagmus",
            "panel_id": 246,
            "panel_version": null,
            "user_name": "Mervyn Thomas",
            "item_type": "entity",
            "text": "reviewed FRMD7",
            "entity_name": "FRMD7",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T20:26:03.219000Z",
            "panel_name": "Infantile nystagmus",
            "panel_id": 246,
            "panel_version": null,
            "user_name": "Mervyn Thomas",
            "item_type": "entity",
            "text": "reviewed CACNA1A",
            "entity_name": "CACNA1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T20:18:42.724000Z",
            "panel_name": "Infantile nystagmus",
            "panel_id": 246,
            "panel_version": null,
            "user_name": "Mervyn Thomas",
            "item_type": "entity",
            "text": "reviewed GPR143",
            "entity_name": "GPR143",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T17:30:02.488000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "panel",
            "text": "promoted panel to version 1",
            "entity_name": null,
            "entity_type": null
        },
        {
            "created": "2016-11-28T17:26:06.629000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified DDB1 as red",
            "entity_name": "DDB1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T17:26:06.628000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on DDB1",
            "entity_name": "DDB1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T17:18:51.320000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked RNF113A as ready",
            "entity_name": "RNF113A",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T17:18:18.183000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified RNF113A as red",
            "entity_name": "RNF113A",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T17:14:07.394000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified MPLKIP as green",
            "entity_name": "MPLKIP",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T17:14:07.393000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on MPLKIP",
            "entity_name": "MPLKIP",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T17:10:29.985000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified GTF2E2 as amber",
            "entity_name": "GTF2E2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T17:07:06.579000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified GTF2E2 as red",
            "entity_name": "GTF2E2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T16:35:51.169000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "added MYH6 to panel",
            "entity_name": "MYH6",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T16:35:50.978000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "reviewed MYH6",
            "entity_name": "MYH6",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T16:23:24.719000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "added ACTC1 to panel",
            "entity_name": "ACTC1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T16:23:24.533000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "reviewed ACTC1",
            "entity_name": "ACTC1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T16:15:40.829000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "classified TBX20 as amber",
            "entity_name": "TBX20",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T16:11:54.584000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "added TBX20 to panel",
            "entity_name": "TBX20",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T16:11:54.402000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "reviewed TBX20",
            "entity_name": "TBX20",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:57:18.193000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked CRELD1 as ready",
            "entity_name": "CRELD1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:56:55.394000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "added CRELD1 to panel",
            "entity_name": "CRELD1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:56:55.222000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "reviewed CRELD1",
            "entity_name": "CRELD1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:43:04.345000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked TBX5 as ready",
            "entity_name": "TBX5",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:42:56.829000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "added TBX5 to panel",
            "entity_name": "TBX5",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:42:56.665000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "reviewed TBX5",
            "entity_name": "TBX5",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:42:02.705000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "added RNF113A to panel",
            "entity_name": "RNF113A",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:42:02.543000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "reviewed RNF113A",
            "entity_name": "RNF113A",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:40:10.989000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "added GTF2E2 to panel",
            "entity_name": "GTF2E2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:40:10.820000Z",
            "panel_name": "Cockayne and Xeroderma Pigmentosum-like disorders",
            "panel_id": 77,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "reviewed GTF2E2",
            "entity_name": "GTF2E2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:36:18.797000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked ELN as ready",
            "entity_name": "ELN",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:36:11.846000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "added ELN to panel",
            "entity_name": "ELN",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:36:11.686000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "reviewed ELN",
            "entity_name": "ELN",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:04:59.687000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked NKX2-5 as ready",
            "entity_name": "NKX2-5",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:04:34.548000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked GATA4 as ready",
            "entity_name": "GATA4",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:04:05.612000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked ZFPM2 as ready",
            "entity_name": "ZFPM2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:04:05.611000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "commented on ZFPM2",
            "entity_name": "ZFPM2",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:01:07.989000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked TBX1 as ready",
            "entity_name": "TBX1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T15:01:07.989000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "commented on TBX1",
            "entity_name": "TBX1",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T14:50:00.545000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked SEMA3D as ready",
            "entity_name": "SEMA3D",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T14:49:44.321000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "reviewed SEMA3D",
            "entity_name": "SEMA3D",
            "entity_type": "gene"
        },
        {
            "created": "2016-11-28T14:47:57.618000Z",
            "panel_name": "Familial non syndromic congenital heart disease",
            "panel_id": 212,
            "panel_version": null,
            "user_name": "Alice Gardham",
            "item_type": "entity",
            "text": "marked NFATC1 as ready",
            "entity_name": "NFATC1",
            "entity_type": "gene"
        }
    ]
}