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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <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#hasRelatedSynonym"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#closeMatch"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0000053 -->

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        <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>
    


    <!-- 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-chr8 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/CHR_9606-chr8">
        <rdfs:label>chromosome 8 (Human)</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019867 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019867">
        <rdfs:label>mosaic trisomy 8</rdfs:label>
        <equivalentClass>
            <Class>
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                        <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/CHR_9606-chr8"/>
                    </Restriction>
                </intersectionOf>
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        </equivalentClass>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0043452"/>
        <rdfs:subClassOf>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/MONDO_0700062"/>
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        </rdfs:subClassOf>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/5359/mosaic-trisomy-8</rdfs:seeAlso>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/mosaic_trisomy_8</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>GARD:0005359</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1096527</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019867</oboInOwl:id>
        <oboInOwl:hasDbXref>SCTID:717335009</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Mosaic trisomy 8 is a chromosomal disorder defined by the presence of three copies of chromosome 8 in some cells of the organism. It is characterized by facial dysmorphism, mild intellectual deficit and joint, urinary, cardiac and skeletal anomalies.</ns4:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>Mosaic trisomy chromosome 8</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Mosaic trisomy type 8</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10053916</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C537940</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:96061</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>trisomy 8 mosaicism</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Warkany syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:797340</oboInOwl:hasDbXref>
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        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/797340"/>
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        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/717335009"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <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_96061"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0043452 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0043452">
        <rdfs:label>chromosome 8, trisomy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700062 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0700062">
        <rdfs:label>mosaic</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0700065 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0700065">
        <rdfs:label>trisomy</rdfs:label>
    </Class>
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