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    <!-- http://purl.obolibrary.org/obo/DOID_3382 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_3382">
        <rdfs:label>liposarcoma</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_5363 -->

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        <rdfs:label>myxoid liposarcoma</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS_CUI:C0206634</oboInOwl:hasDbXref>
        <rdfs:comment>OMIM mapping confirmed by DO. [SN].</rdfs:comment>
        <oboInOwl:hasDbXref>OMIM:613488</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ORDO:99967</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D018208</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:7157</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym xml:lang="en">Myxoid/round cell liposarcoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <ns2:IAO_0000115>A liposarcoma that is characterized by the presence of a hypocellular spindle cell proliferation set in a myxoid background and has_material_basis_in chromosomal translocations.</ns2:IAO_0000115>
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