<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/BTO?iri=http://purl.obolibrary.org/obo/BTO_0005830"?>
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     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
     xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:ns4="http://purl.obolibrary.org/obo/"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
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    //
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasOBONamespace"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#created_by"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004025 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004025">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">disease causes dysfunction of</rdfs:label>
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/BTO_0000236 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/BTO_0000236">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">cerebral white matter</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/BTO_0005830 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/BTO_0005830">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">leukodystrophy disease specific cell type</rdfs:label>
        <rdfs:subClassOf>
            <Restriction>
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        <oboInOwl:creation_date rdf:datatype="http://www.w3.org/2001/XMLSchema#string">2016-04-18T09:29:37Z</oboInOwl:creation_date>
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        <oboInOwl:hasOBONamespace rdf:datatype="http://www.w3.org/2001/XMLSchema#string">BrendaTissueOBO</oboInOwl:hasOBONamespace>
        <ns4:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Leukodystrophy is a term for a group of white matter diseases, some familial, characterized by progressive cerebral deterioration usually in early life, and pathologically by primary absence or degeneration of the myelin of the central and peripheral nervous systems with glial reaction; probably related to a defect in lipid metabolism.</ns4:IAO_0000115>
        <oboInOwl:created_by rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Marion, contact@brenda-enzymes.org</oboInOwl:created_by>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



