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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004030 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004030">
        <rdfs:label>disease arises from structure</rdfs:label>
        <rdfs:label>disease arises from alteration in structure</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/CHR_9606-chrXq25 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/CHR_9606-chrXq25">
        <rdfs:label>Xq25 (Human)</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000762 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000762">
        <rdfs:label>syndrome caused by partial chromosomal duplication</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010507 -->

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        <rdfs:label>Xq25 microduplication syndrome</rdfs:label>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/CHR_9606-chrXq25"/>
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        </rdfs:subClassOf>
        <ns7:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3492</ns7:IAO_0000233>
        <ns7:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns7:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/chromosome_xq25_duplication_syndrome</ns3:curated_content_resource>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/xq25_microduplication_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C4311049</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0010507</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0017955</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:300979</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:935016</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C177544</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Xq25 duplication syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:521258</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Xq25 triplication syndrome</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015159 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015159">
        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017010 -->

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        <rdfs:label>partial duplication of the long arm of chromosome X</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020119 -->

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        <rdfs:label>X-linked syndromic intellectual disability</rdfs:label>
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