NCPI FHIR Implementation Guide v2
0.1.0 - ci-build

NCPI FHIR Implementation Guide v2 - Local Development build (v0.1.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

: The Centers for Medelian Genetics - JSON Representation

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{
  "resourceType" : "List",
  "id" : "ncpi-research-collection-cmg",
  "meta" : {
    "profile" : [
      🔗 "https://nih-ncpi.github.io/ncpi-fhir-ig-2/StructureDefinition/ncpi-research-collection"
    ]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><h2>The Centers for Medelian Genetics</h2><table class=\"clstu\"><tr><td>Mode: snapshotStatus: currentCode: Consortium</td></tr><tr><td/></tr></table><table class=\"grid\"><tr style=\"backgound-color: #eeeeee\"><td><b>Items</b></td></tr><tr><td><a href=\"ResearchStudy-cmg-research-study-bhcmg.html\">ResearchStudy/cmg-research-study-bhcmg</a></td></tr></table></div>"
  },
  "extension" : [
    {
      "url" : "https://nih-ncpi.github.io/ncpi-fhir-ig-2/StructureDefinition/research-web-Link",
      "valueUrl" : "https://mendeliangenomics.org/"
    },
    {
      "extension" : [
        {
          "url" : "type",
          "valueCodeableConcept" : {
            "coding" : [
              {
                "system" : "http://terminology.hl7.org/CodeSystem/title-type",
                "code" : "acronym"
              }
            ]
          }
        },
        {
          "url" : "label",
          "valueString" : "CMG"
        }
      ],
      "url" : "https://nih-ncpi.github.io/ncpi-fhir-ig-2/StructureDefinition/label-extension"
    }
  ],
  "status" : "current",
  "mode" : "snapshot",
  "title" : "The Centers for Medelian Genetics",
  "code" : {
    "coding" : [
      {
        "system" : "https://nih-ncpi.github.io/ncpi-fhir-ig-2/CodeSystem/collection-type",
        "code" : "consortium",
        "display" : "Consortium"
      }
    ]
  },
  "note" : [
    {
      "text" : "The Centers for Mendelian Genomics project uses next-generation sequencing and computational approaches to discover the genes and variants that underlie Mendelian conditions. By discovering genes that cause Mendelian conditions, we will expand our understanding of their biology to facilitate diagnosis and new treatments."
    }
  ],
  "entry" : [
    {
      "item" : {
        🔗 "reference" : "ResearchStudy/cmg-research-study-bhcmg"
      }
    }
  ]
}