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    <!-- http://www.ebi.ac.uk/efo/EFO_0000515 -->

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        <rdfs:label>obsolete_brain tumor glioblastoma</rdfs:label>
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        <ns2:IAO_0000115>A rare histological variant of glioblastoma (WHO grade IV) with a predominance of bizarre, multinucleated giant cells, an occasionally abundant stromal reticulin network, and a high frequency of TP53 mutations. (WHO)</ns2:IAO_0000115>
        <ns2:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0018177</ns2:IAO_0100001>
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        <ns5:reason_for_obsolescence>duplication with glioblastoma (EFO_0000519)</ns5:reason_for_obsolescence>
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        <oboInOwl:hasDbXref>NCIt:C4325</oboInOwl:hasDbXref>
        <ns2:IAO_0000117>James Malone</ns2:IAO_0000117>
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        <oboInOwl:hasDbXref>MESH:D005909</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures.</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>DOID:3074</oboInOwl:hasDbXref>
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