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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/UPHENO_0000001 -->

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        <rdfs:label>phenotype affects entity</rdfs:label>
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    <!-- 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_0011792"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/UPHENO_0000001"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/MPATH_74"/>
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        <oboInOwl:creation_date>2009-10-16T02:51:16Z</oboInOwl:creation_date>
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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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    <!-- http://purl.obolibrary.org/obo/HP_0011792 -->

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        <rdfs:label>Neoplasm by histology</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MPATH_74 -->

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        <rdfs:label>hamartoma</rdfs:label>
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