<?xml version="1.0"?>
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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/SCDO_1000288"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/SCDO_0000303"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/SCDO_0000340"/>
    


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    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
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    <!-- http://purl.obolibrary.org/obo/SCDO_0000527 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/SCDO_0000527">
        <rdfs:label>Hemoglobin D-Ibadan</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/SCDO_1000259"/>
        <oboInOwl:hasExactSynonym>Hemoglobin D (badan)</oboInOwl:hasExactSynonym>
        <ns2:SCDO_1000288>Few but definitions not freely available</ns2:SCDO_1000288>
        <ns2:IAO_0000115>An unusual hemoglobin that shows all the electrophoretic features of Hb D, but has no inherited disability. This hemoglobin has a beta 87 Thr &gt; Lys mutation.</ns2:IAO_0000115>
        <ns2:SCDO_0000303>Request inclusion into NCIT below &quot;Hemoglobin&quot;/&quot;Hemoglobin Variant&quot;/&quot;Unusual Hemoglobin&quot;.</ns2:SCDO_0000303>
        <ns2:SCDO_0000340 rdf:resource="http://dx.doi.org/10.1038/2051273a0"/>
        <ns2:SCDO_0000340 rdf:resource="https://www.omim.org/entry/141900#0062"/>
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    <!-- http://purl.obolibrary.org/obo/SCDO_1000259 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/SCDO_1000259">
        <rdfs:label>Unusual Hemoglobin</rdfs:label>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



