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        <rdfs:label xml:lang="en">has characteristic</rdfs:label>
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    <!-- http://identifiers.org/hgnc/9688 -->

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        <rdfs:label>CAVIN1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005015 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005015">
        <rdfs:label>diabetes mellitus</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005336 -->

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        <rdfs:label>myopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006536 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006536">
        <rdfs:label>congenital generalized lipodystrophy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0013225 -->

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        <rdfs:label>congenital generalized lipodystrophy type 4</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4069</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5723</ns5:IAO_0000233>
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        <oboInOwl:hasDbXref>OMIM:613327</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>Any congenital generalized lipodystrophy in which the cause of the disease is a mutation in the CAVIN1 gene.</ns5:IAO_0000115>
        <oboInOwl:hasExactSynonym>BSCL4</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021140 -->

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