<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0019779"?>
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     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:mondo="http://purl.obolibrary.org/obo/mondo#"
     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#"
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     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000231"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
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    <!-- 
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    //
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010663 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010663">
        <rdfs:label>intellectual disability-hypotonic facies syndrome, X-linked, 1</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019779 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019779">
        <rdfs:label>obsolete Renier-Gabreels-Jasper syndrome</rdfs:label>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5061</ns4:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/4672/renier-gabreels-jasper-syndrome</rdfs:seeAlso>
        <deprecated rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</deprecated>
        <oboInOwl:hasDbXref>SCTID:723501008</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:93975</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019779</oboInOwl:id>
        <ns4:IAO_0000115>OBSOLETE. Renier-Gabreels-Jasper syndrome is an X-linked mental retardation (XLMR) syndrome belonging to the group of conditions characterized by the association of intellectual deficit with hypotonic facies (Mental retardation, X-linked-hypotonic facies).</ns4:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>Renier Gabreels Jasper syndrome</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:consider rdf:resource="http://purl.obolibrary.org/obo/MONDO_0010663"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_93975"/>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



