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

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        <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-chr4q25 -->

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        <rdfs:label>4q25 (Human)</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015160 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016903 -->

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        <rdfs:label>partial deletion of the long arm of chromosome 4</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0044717 -->

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        <rdfs:label>4q25 proximal deletion syndrome</rdfs:label>
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        <oboInOwl:id>MONDO:0044717</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0022048</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:502437</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:1814447</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>proximal monosomy 4q25</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>proximal del(4)(q25)</oboInOwl:hasExactSynonym>
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