<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EPIO?iri=http://purl.obolibrary.org/obo/DOID_1825"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     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:ns2="http://purl.obolibrary.org/obo/"
     xmlns:ns4="https://bio.scai.fraunhofer.de/ontology/epilepsy#"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="https://bio.scai.fraunhofer.de/ontology/epilepsy#fromEpSO"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="https://bio.scai.fraunhofer.de/ontology/epilepsy#fromILAE"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="https://bio.scai.fraunhofer.de/ontology/epilepsy#fromESSO"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasOBONamespace"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="https://bio.scai.fraunhofer.de/ontology/epilepsy#fromEPILONT"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDefinition"/>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Datatypes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- http://purl.obolibrary.org/obo/DOID_1825 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_1825">
        <rdfs:label>childhood absence epilepsy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_1827"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020072"/>
        <ns4:fromEPILONT rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns4:fromEPILONT>
        <ns4:fromILAE rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns4:fromILAE>
        <ns4:fromESSO rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns4:fromESSO>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2018_03_01:16757004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>CSP2005:0485-7316</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D004832</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCI:C3023</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2018_03_01:79631006</oboInOwl:hasDbXref>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasExactSynonym>pyknolepsy</oboInOwl:hasExactSynonym>
        <ns2:IAO_0000115>A childhood electroclinical syndrome that is characterized by brief and frequent absence seizures in children with age of onset between four and ten years.</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS_CUI:C0014553</oboInOwl:hasDbXref>
        <oboInOwl:id>DOID:1825</oboInOwl:id>
        <rdfs:seeAlso>http://www.case.edu/EpSO.owl#ChildhoodAbsenceEpilepsy</rdfs:seeAlso>
        <oboInOwl:hasRelatedSynonym>absence seizure</oboInOwl:hasRelatedSynonym>
        <ns4:fromEpSO></ns4:fromEpSO>
        <oboInOwl:hasExactSynonym>petit mal seizure</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDefinition>Childhood absence epilepsy is a genetic/idiopathic generalized epilepsy that should be considered in an otherwise normal child with multiple daily absence seizures associated with 2.5 - 3.5 Hz generalized spike-and-wave. Absence seizures are provoked by hyperventilation. Between 8 and 12 years of age the distinction between the clinical syndromes of juvenile absence epilepsy and childhood absence epilepsy depends on the frequency of absence seizures.</oboInOwl:hasDefinition>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/doid#NCIthesaurus"/>
        <ns2:IAO_0000412 rdf:resource="http://purl.obolibrary.org/obo/doid.owl"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/DOID_1827 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_1827">
        <rdfs:label>idiopathic generalized epilepsy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020072 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020072">
        <rdfs:label>childhood-onset epilepsy syndrome</rdfs:label>
    </Class>
</rdf:RDF>



<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



