<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EFO?iri=http://www.ebi.ac.uk/efo/EFO_0700136"?>
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     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:ns5="http://www.ebi.ac.uk/efo/"
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     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#"
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     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
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    <AnnotationProperty rdf:about="http://www.ebi.ac.uk/efo/reason_for_obsolescence"/>
    <AnnotationProperty rdf:about="http://www.ebi.ac.uk/efo/obsoleted_in_version"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0100001"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    


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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
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    <!-- http://www.ebi.ac.uk/efo/EFO_0700136 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0700136">
        <rdfs:label>obsolete_apolipoprotein A-I deficiency</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.w3.org/2002/07/owl#Thing"/>
        <deprecated rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</deprecated>
        <oboInOwl:hasExactSynonym>familial hypoalphalipoproteinemia</oboInOwl:hasExactSynonym>
        <rdfs:comment>Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also.</rdfs:comment>
        <oboInOwl:hasDbXref>Orphanet:425</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A rare lipoprotein metabolism disorder characterized biochemically by complete absence of apolipoprotein AI and extremely low plasma high density lipoprotein (HDL) cholesterol, and clinically by corneal opacities and xanthomas complicated with premature coronary heart disease (CHD).</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>familial apoA-I deficiency</oboInOwl:hasExactSynonym>
        <ns4:IAO_0100001>http://purl.obolibrary.org/obo/MONDO_0700513</ns4:IAO_0100001>
        <oboInOwl:hasExactSynonym>ApoA-I deficiency</oboInOwl:hasExactSynonym>
        <ns5:obsoleted_in_version>3.88.0</ns5:obsoleted_in_version>
        <ns5:reason_for_obsolescence>Replaced by Mondo term MONDO_0700513, with which this term was previously merged. Use: http://purl.obolibrary.org/obo/MONDO_0700513</ns5:reason_for_obsolescence>
    </Class>
</rdf:RDF>



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



