<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_1012901"?>
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     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: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
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <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"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    


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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004003">
        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
    </ObjectProperty>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
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    <!-- http://identifiers.org/ncbigene/516891 -->

    <Class rdf:about="http://identifiers.org/ncbigene/516891">
        <rdfs:label>FA2H</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_1011321 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_1011321">
        <rdfs:label>hereditary disease, non-human animal</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_1011541 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_1011541">
        <rdfs:label>ichthyosis, cattle</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_1012901 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_1012901">
        <rdfs:label>ichthyosis, FA2H-related, cattle</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_1011321"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_1011541"/>
        <rdfs:subClassOf>
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                <someValuesFrom rdf:resource="http://identifiers.org/ncbigene/516891"/>
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        </rdfs:subClassOf>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/7271</ns4:IAO_0000233>
        <oboInOwl:id>MONDO:1012901</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIA:002450-9913</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Ichthyosis that occurs in cattle due to a mutation in the FA2H gene.</ns4:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>ichthyosis congenita, cattle</oboInOwl:hasRelatedSynonym>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



