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    <!-- http://purl.obolibrary.org/obo/NCIT_C165258 -->

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        <rdfs:label>Cellosaurus Disease Terminology</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C207968 -->

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        <rdfs:label>SMCHD1 Gene</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C219543 -->

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        <rdfs:label>LRIF1 Gene</rdfs:label>
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        <rdfs:label>DNMT3B Gene</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C84704 -->

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        <rdfs:label>Facioscapulohumeral Muscular Dystrophy</rdfs:label>
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        <ns2:NCIT_P207>C0238288</ns2:NCIT_P207>
        <ns2:NCIT_P108>Facioscapulohumeral Muscular Dystrophy</ns2:NCIT_P108>
        <ns2:IAO_0000115>An autosomal dominant disorder affecting the skeletal muscles of the face, scapula, and upper arm. Patients present with muscle weakness in these anatomic areas. The muscle weakness eventually spreads to other skeletal muscles as well.</ns2:IAO_0000115>
        <ns2:NCIT_P322>Cellosaurus</ns2:NCIT_P322>
        <ns2:NCIT_NHC0>C84704</ns2:NCIT_NHC0>
        <ns2:NCIT_P106>Disease or Syndrome</ns2:NCIT_P106>
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        <rdfs:label>Muscular Dystrophy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C97463 -->

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        <rdfs:label>DUX4 Gene</rdfs:label>
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