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     xmlns:efo="http://www.ebi.ac.uk/efo/">
    


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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017704 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017704">
        <rdfs:label>familial partial epilepsy</rdfs:label>
    </Class>
    


    <!-- http://www.ebi.ac.uk/efo/EFO_0700037 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0700037">
        <rdfs:label>benign familial mesial temporal lobe epilepsy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0017704"/>
        <oboInOwl:hasDbXref>Orphanet:163717</oboInOwl:hasDbXref>
        <rdfs:comment>Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also.</rdfs:comment>
        <oboInOwl:hasExactSynonym>benign FMTLE</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:CN226709</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Benign familial mesial temporal lobe epilepsy is a rare epilepsy characterized by seizures with viscerosensory or experential auras, onset in adolescence or early adulthood and good prognosis. It is defined as at least 24 months of seizure freedom with or without antiepileptic medication.</ns3:IAO_0000115>
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