<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EPIO?iri=http://purl.obolibrary.org/obo/MONDO_0044970"?>
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     xmlns:ns4="https://bio.scai.fraunhofer.de/ontology/epilepsy#"
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     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
    <AnnotationProperty rdf:about="https://bio.scai.fraunhofer.de/ontology/epilepsy#fromILAE"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDefinition"/>
    


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    <!-- http://purl.obolibrary.org/obo/MONDO_0044970 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0044970">
        <rdfs:label>mitochondrial disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="https://bio.scai.fraunhofer.de/ontology/epilepsy#metabolic_etiology"/>
        <ns4:fromILAE rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns4:fromILAE>
        <rdfs:seeAlso>https://www.epilepsydiagnosis.org/aetiology/metabolic-groupoverview.html#mitochondrial</rdfs:seeAlso>
        <oboInOwl:id>MONDO:0044970</oboInOwl:id>
        <oboInOwl:hasDefinition>Mitochondrial diseases (MIDs) are a large group of heterogeneous disorders due to mutations in either mitochondrial DNA (mtDNA) or nuclear DNA (nDNA) genes, the latter encoding proteins involved in mitochondrial function.</oboInOwl:hasDefinition>
        <ns2:IAO_0000412 rdf:resource="http://purl.obolibrary.org/obo/mondo.owl"/>
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    <!-- https://bio.scai.fraunhofer.de/ontology/epilepsy#metabolic_etiology -->

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        <rdfs:label>metabolic etiology</rdfs:label>
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