<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EFO?iri=http://purl.obolibrary.org/obo/MONDO_0019587"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
     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#"
     xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:ORDO="http://www.orpha.net/ORDO/"
     xmlns:ns2="http://purl.obolibrary.org/obo/mondo#"
     xmlns:ns4="http://purl.obolibrary.org/obo/"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#excluded_subClassOf"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasNarrowSynonym"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasBroadSynonym"/>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Datatypes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- 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_0016297 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016297">
        <rdfs:label>prelingual non-syndromic genetic hearing loss</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016298 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016298">
        <rdfs:label>postlingual non-syndromic genetic hearing loss</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019497 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019497">
        <rdfs:label>nonsyndromic genetic hearing loss</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019587 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019587">
        <rdfs:label>autosomal dominant nonsyndromic hearing loss</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000426"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019497"/>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/551</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/7621</ns4:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/autosomal_dominant_nonsyndromic_deafness</ns2:curated_content_resource>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/rare_autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>DOID:0050564</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>autosomal dominant nonsyndromic hearing loss</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C5779548</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>autosomal dominant non-syndromic sensorineural deafness type DFNA</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasBroadSynonym>autosomal dominant deafness</oboInOwl:hasBroadSynonym>
        <ns4:IAO_0000115>Autosomal dominant form of nonsyndromic deafness.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>autosomal dominant non-syndromic sensorineural hearing loss type DFNA</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>autosomal dominant nonsyndromic hearing impairment</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0016791</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>nonsyndromic genetic deafness, autosomal dominant</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>autosomal dominant isolated deafness</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>autosomal dominant non-syndromic neurosensory deafness type DFNA</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasExactSynonym>autosomal dominant non-syndromic neurosensory hearing loss type DFNA</oboInOwl:hasExactSynonym>
        <oboInOwl:hasNarrowSynonym>autosomal dominant nonsyndromic genetic deafness</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>deafness, autosomal dominant</oboInOwl:hasNarrowSynonym>
        <oboInOwl:id>MONDO:0019587</oboInOwl:id>
        <oboInOwl:hasNarrowSynonym>autosomal dominant nonsyndromic hearing loss and deafness</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>nonsyndromic deafness, autosomal dominant</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>autosomal dominant nonsyndromic deafness</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>autosomal dominant isolated neurosensory deafness type DFNA</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>MEDGEN:1843285</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>autosomal dominant isolated neurosensory hearing loss type DFNA</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIMPS:124900</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>autosomal dominant isolated sensorineural hearing loss type DFNA</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:90635</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>autosomal dominant isolated sensorineural deafness type DFNA</oboInOwl:hasNarrowSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/1843285"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C5779548"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0050564"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016297"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016298"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#clingen"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <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#ordo_etiological_subtype"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_subtype_of_a_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_90635"/>
        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS124900"/>
        <ns2:curated_content_resource rdf:resource="https://search.clinicalgenome.org/kb/conditions/MONDO:0019587"/>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_90635 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_90635">
        <rdfs:label>obsolete_Autosomal dominant non-syndromic sensorineural deafness type DFNA</rdfs:label>
    </Class>
</rdf:RDF>



<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



