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     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
     xmlns:skos="http://www.w3.org/2004/02/skos/core#"
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     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/"
     xmlns:ns3="http://purl.obolibrary.org/obo/mondo#">
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
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     -->

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007030 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007030">
        <rdfs:label>autosomal dominant Aarskog syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000426"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021005"/>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/autosomal_dominant_aarskog_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasDbXref>GARD:0015029</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C3149220</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007030</oboInOwl:id>
        <oboInOwl:hasDbXref>NORD:702</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0111825</oboInOwl:hasDbXref>
        <rdfs:comment>We place the DO class here as it is explicitly AD, but it&#39;s not clear if the intent is for the DO class to be equivalent to the classic X-linked form (the DO synonyms suggest this is the case)</rdfs:comment>
        <oboInOwl:hasRelatedSynonym>Aarskog Syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:100050</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:460570</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/460570"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C3149220"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0111825"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/100050"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0021005 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021005">
        <rdfs:label>faciodigitogenital syndrome</rdfs:label>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



