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    <!-- http://purl.obolibrary.org/obo/MONDO_0000761 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000761">
        <rdfs:label>syndrome caused by partial chromosomal deletion</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016911 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016911">
        <rdfs:label>partial deletion of the long arm of chromosome 13</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000761"/>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3664</ns3:IAO_0000233>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/partial_deletion_of_the_long_arm_of_chromosome_13_syndrome</ns4:curated_content_resource>
        <oboInOwl:id>MONDO:0016911</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:262101</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>partial deletion of chromosome 13q</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>partial monosomy of chromosome 13q</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>13q deletion</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>13q monosomy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NCIT:C36497</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>chromosome 13q deletion</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>partial deletion of the long arm of chromosome type 13</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>monosomy 13q</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>deletion 13q</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C0265451</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:120541</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A cytogenetic abnormality that refers to the allelic loss of all or part of the long arm of chromosome 13.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:C535449</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>partial monosomy of the long arm of chromosome 13</oboInOwl:hasExactSynonym>
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        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_262101"/>
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        <rdfs:label>obsolete_partial deletion of the long arm of chromosome 13</rdfs:label>
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