<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0019934"?>
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     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:ns5="http://purl.obolibrary.org/obo/mondo#"
     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: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#disease_grouping"/>
    <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"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
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    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    


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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0000053">
        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#InverseFunctionalProperty"/>
        <rdfs:label>has characteristic</rdfs:label>
        <rdfs:label xml:lang="en">has characteristic</rdfs:label>
    </ObjectProperty>
    


    <!-- 
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    //
    // Classes
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019040 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019040">
        <rdfs:label>chromosomal disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019934 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019934">
        <rdfs:label>polyploidy</rdfs:label>
        <equivalentClass>
            <Class>
                <intersectionOf rdf:parseType="Collection">
                    <rdf:Description rdf:about="http://purl.obolibrary.org/obo/MONDO_0019040"/>
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                        <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/SO_0001254"/>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019040"/>
        <rdfs:subClassOf>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/SO_0001254"/>
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        </rdfs:subClassOf>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/polyploidy_syndrome</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>MESH:D011123</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:96321</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Chromosomal disorder in which the chromosomal constitution of a cell containing multiples of the normal number of chromosomes; includes triploidy (symbol: 3N), tetraploidy (symbol: 4N), etc.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>icd11.foundation:1286128770</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0019348</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019934</oboInOwl:id>
        <oboInOwl:hasDbXref>UMLS:C0032578</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:18567</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:72991005</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/1286128770"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/18567"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D011123"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/72991005"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0032578"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#disease_grouping"/>
        <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_group_of_disorders"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_96321"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/SO_0001254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/SO_0001254">
        <rdfs:label>polyploid</rdfs:label>
    </Class>
</rdf:RDF>



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



