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     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004026 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004026">
        <rdfs:label>disease has location</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/mondo#disease_has_basis_in_development_of -->

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        <rdfs:label>disease_has_basis_in_development_of</rdfs:label>
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        <rdfs:label>disease has major feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0000202 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000202">
        <rdfs:label>Orofacial cleft</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000358 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000358">
        <rdfs:label>orofacial cleft</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0023369"/>
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        </rdfs:subClassOf>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/orofacial_cleft</ns5:curated_content_resource>
        <oboInOwl:id>MONDO:0000358</oboInOwl:id>
        <oboInOwl:hasDbXref>UMLS:C3266076</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:119530</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0050567</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A disorder of facial skeleton that is characterized by cleft lip and/or cleft palate that result in feeding, speech and hearing problems caused by failures during development.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>SCTID:449790007</oboInOwl:hasDbXref>
        <rdfs:comment>Editor notes: most subtypes are isolated</rdfs:comment>
        <oboInOwl:hasDbXref>MEDGEN:472000</oboInOwl:hasDbXref>
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        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS119530"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003847">
        <rdfs:label>hereditary disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0023369 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0023369">
        <rdfs:label>disorder of facial skeleton</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/UBERON_0001456 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/UBERON_0001456">
        <rdfs:label>face</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/UBERON_0012314 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/UBERON_0012314">
        <rdfs:label>embryonic facial prominence</rdfs:label>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



