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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/HP_0000118 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000118">
        <rdfs:label>Phenotypic abnormality</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0010566 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0010566">
        <rdfs:label>Hamartoma</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0000118"/>
        <dcterms:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2009-10-16T02:51:16Z</dcterms:date>
        <ns2:gwas_trait rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns2:gwas_trait>
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        <oboInOwl:hasDbXref>SNOMEDCT_US:400006008</oboInOwl:hasDbXref>
        <oboInOwl:id>HP:0010566</oboInOwl:id>
        <ns4:IAO_0000115>A disordered proliferation of mature tissues that is native to the site of origin, e.g., exostoses, nevi and soft tissue hamartomas. Although most hamartomas are benign, some histologic subtypes, e.g., neuromuscular hamartoma, may proliferate aggressively such as mesenchymal cystic hamartoma, Sclerosing epithelial hamartoma, Sclerosing metanephric hamartoma.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>SNOMEDCT_US:51398009</oboInOwl:hasDbXref>
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