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 - XML Representation

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<List xmlns="http://hl7.org/fhir">
  <id value="ncpi-research-collection-cmg"/>
  <meta>
    <profile
             value="https://nih-ncpi.github.io/ncpi-fhir-ig-2/StructureDefinition/ncpi-research-collection"/>
  </meta>
  <text>
    <status value="generated"/>
    <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>
  </text>
  <extension
             url="https://nih-ncpi.github.io/ncpi-fhir-ig-2/StructureDefinition/research-web-Link">
    <valueUrl value="https://mendeliangenomics.org/"/>
  </extension>
  <extension
             url="https://nih-ncpi.github.io/ncpi-fhir-ig-2/StructureDefinition/label-extension">
    <extension url="type">
      <valueCodeableConcept>
        <coding>
          <system value="http://terminology.hl7.org/CodeSystem/title-type"/>
          <code value="acronym"/>
        </coding>
      </valueCodeableConcept>
    </extension>
    <extension url="label">
      <valueString value="CMG"/>
    </extension>
  </extension>
  <status value="current"/>
  <mode value="snapshot"/>
  <title value="The Centers for Medelian Genetics"/>
  <code>
    <coding>
      <system
              value="https://nih-ncpi.github.io/ncpi-fhir-ig-2/CodeSystem/collection-type"/>
      <code value="consortium"/>
      <display value="Consortium"/>
    </coding>
  </code>
  <note>
    <text
          value="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."/>
  </note>
  <entry>
    <item>🔗 
      <reference value="ResearchStudy/cmg-research-study-bhcmg"/>
    </item>
  </entry>
</List>