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    <!-- http://purl.obolibrary.org/obo/MONDO_0002728 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002728">
        <rdfs:label>rhabdoid tumor</rdfs:label>
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        <ns3:IAO_0000115>An aggressive malignant embryonal neoplasm usually occurring during childhood. It is characterized by the presence of large cells with abundant cytoplasm, large eccentric nucleus, and a prominent nucleolus and it is associated with abnormalities of chromosome 22. It can arise from the central nervous system, kidney, and the soft tissues. The prognosis is poor.</ns3:IAO_0000115>
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        <oboInOwl:id>MONDO:0002728</oboInOwl:id>
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        <oboInOwl:hasDbXref>ICDO:8963/3</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>GARD:0007572</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:69077</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:3672</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>rhabdoid sarcoma</oboInOwl:hasExactSynonym>
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        <rdfs:label>embryonal neoplasm</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018078 -->

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        <rdfs:label>soft tissue sarcoma</rdfs:label>
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