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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    


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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/RO_0004021 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004021">
        <rdfs:label>disease has basis in disruption of</rdfs:label>
        <rdfs:label>disease caused by disruption of</rdfs:label>
    </ObjectProperty>
    


    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004029">
        <rdfs:label>disease has feature</rdfs:label>
    </ObjectProperty>
    


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    <!-- http://purl.obolibrary.org/obo/GO_0009235 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/GO_0009235">
        <rdfs:label>cobalamin metabolic process</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0100502 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0100502">
        <rdfs:label>Decreased circulating vitamin B12 concentration</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005066 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005066">
        <rdfs:label>metabolic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020696 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020696">
        <rdfs:label>vitamin B12 deficiency</rdfs:label>
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        </rdfs:subClassOf>
        <oboInOwl:hasDbXref>icd11.foundation:1366882206</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0042847</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hypocobalaminemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C131684</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>HP:0100502</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>EFO:0000734</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0020696</oboInOwl:id>
        <oboInOwl:hasDbXref>ICD9:266.2</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>vitamin b12 deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D014806</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:190634004</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A disease characterized by low serum levels of vitamin B12, either inherited or acquired.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>cobalamin deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:21880</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0042976 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0042976">
        <rdfs:label>vitamin B deficiency</rdfs:label>
    </Class>
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