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    <!-- http://purl.obolibrary.org/obo/HP_0031459 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0031459">
        <rdfs:label>Soft tissue neoplasm</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_6001034 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_6001034">
        <rdfs:label>Desmoid tumor</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0031459"/>
        <dcterms:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2024-07-18T14:41:44Z</dcterms:date>
        <oboInOwl:hasExactSynonym>Desmoid-type fibromatosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Aggressive fibromatosis</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>Desmoid tumors are rare, locally aggressive, fibroblastic soft-tissue tumors that are characterized by infiltrative growth and tendency to recur. Desmoid tumors do not metastasize but can arise in any part of the body: extra-abdominal (appear in the head and neck, chest, extremities), and abdominal wall or intra-abdominal (originating in tissue that connects abdominal organs).</ns4:IAO_0000115>
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