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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://purl.org/dc/terms/creator"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#inferred_rare"/>
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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-chr21 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/CHR_9606-chr21">
        <rdfs:label>chromosome 21 (Human)</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008608 -->

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        <rdfs:label>Down syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700065 -->

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        <rdfs:label>trisomy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700126 -->

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        <rdfs:label>trisomy 21</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C3537167</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:760825</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>A chromosomal disorder consisting of the presence of an extra chromosome 21.</ns5:IAO_0000115>
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        <dcterms:creator rdf:resource="https://orcid.org/0000-0002-4142-7153"/>
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