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    <!-- http://purl.obolibrary.org/obo/NCIT_C102891 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/NCIT_C102891">
        <rdfs:label>SOX10 Gene</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C165258 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/NCIT_C165258">
        <rdfs:label>Cellosaurus Disease Terminology</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C21112 -->

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        <rdfs:label>KITLG Gene</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C50877 -->

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        <rdfs:label>SNAI2 Gene</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C70584 -->

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        <rdfs:label>MITF Gene</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C75009 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/NCIT_C75009">
        <rdfs:label>Waardenburg Syndrome Type 2</rdfs:label>
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        <ns2:NCIT_P108>Waardenburg Syndrome Type 2</ns2:NCIT_P108>
        <ns2:IAO_0000115>A rare autosomal dominant syndrome caused by mutations in the MITF and SNAI2 genes. It has all of the features of Waardenburg syndrome Type 1 except dystopia canthorum.</ns2:IAO_0000115>
        <ns2:NCIT_P207>C2700265</ns2:NCIT_P207>
        <oboInOwl:hasExactSynonym>Waardenburg Syndrome Type II</oboInOwl:hasExactSynonym>
        <ns2:NCIT_NHC0>C75009</ns2:NCIT_NHC0>
        <oboInOwl:hasExactSynonym>Waardenburg Syndrome Type 2</oboInOwl:hasExactSynonym>
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        <ns2:NCIT_P322>Cellosaurus</ns2:NCIT_P322>
        <ns2:NCIT_P366>Waardenburg_Syndrome_Type_2</ns2:NCIT_P366>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C85222 -->

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