<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0023186"?>
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     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:obo="http://purl.obolibrary.org/obo/"
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    <!-- 
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004029">
        <rdfs:label>disease has feature</rdfs:label>
    </ObjectProperty>
    


    <!-- 
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005516 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005516">
        <rdfs:label>osteochondrodysplasia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0010029 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010029">
        <rdfs:label>situs inversus</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0023186 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0023186">
        <rdfs:label>Fraser Jequier Chen syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005516"/>
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        </rdfs:subClassOf>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/2373/fraser-jequier-chen-syndrome</rdfs:seeAlso>
        <oboInOwl:hasDbXref>MEDGEN:419665</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0023186</oboInOwl:id>
        <oboInOwl:hasDbXref>MESH:C535481</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C2930912</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>chondrodysplasia, situs inversus totalis, cleft epiglottis and larynx, hexadactyly of hands and feet, pancreatic cystic dysplasia, renal dysplasia/abs</oboInOwl:hasRelatedSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/419665"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C535481"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C2930912"/>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



