<?xml version="1.0"?>
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     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.org/dc/terms/creator"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.org/dc/terms/date"/>
    


    <!-- 
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/HP_0002859 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0002859">
        <rdfs:label>Rhabdomyosarcoma</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0500092 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0500092">
        <rdfs:label>Orbital rhabdomyosarcoma</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0002859"/>
        <dcterms:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2018-03-27T15:11:41Z</dcterms:date>
        <ns2:IAO_0000115>A mesenchymal tumor that is considered to be the commonest primary orbital malignancy in children. Histologically, it may be differentiated into embryonal, alveolar, and pleomorphic types. It is usually intraconal or within the superior orbit.</ns2:IAO_0000115>
        <dcterms:creator rdf:resource="https://orcid.org/0000-0001-7941-2961"/>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



