<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0018075"?>
<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:skos="http://www.w3.org/2004/02/skos/core#"
     xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:ns2="http://purl.obolibrary.org/obo/mondo#"
     xmlns:ns4="http://purl.obolibrary.org/obo/"
     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/mondo#disease_grouping"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#excluded_subClassOf"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ncit_rare"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015219 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015219">
        <rdfs:label>obsolete non-syndromic central nervous system malformation</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018075 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018075">
        <rdfs:label>neural tube defect</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020022"/>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/neural_tube_defects</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>MESH:D009436</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0080074</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C84923</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:18009</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A congenital defect characterized by failure of the neural tube to close completely; this results in the presence of openings in the brain or spinal cord. Examples of neural tube defects include encephalocele and spina bifida.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>ICD9:742.8</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>spinal dysraphism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:253098009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0027794</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0018796</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0018075</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:3388</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>NTD</oboInOwl:hasExactSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/18009"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D009436"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/253098009"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0027794"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0080074"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015219"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019117"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C84923"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#disease_grouping"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ncit_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_3388"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019117 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019117">
        <rdfs:label>obsolete genetic nervous system disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020022 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020022">
        <rdfs:label>central nervous system malformation</rdfs:label>
    </Class>
</rdf:RDF>



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



