<?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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    <!-- http://purl.obolibrary.org/obo/SCDO_0001386 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/SCDO_0001386">
        <rdfs:label>Alpha-Globin Locus Deletion</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/SCDO_0008251 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/SCDO_0008251">
        <rdfs:label>Homozygous Deletion of HBA1</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/SCDO_0001386"/>
        <dc:creator>SCDO (Jade Hotchkiss)</dc:creator>
        <oboInOwl:hasExactSynonym>Trans Deletion of HBA1</oboInOwl:hasExactSynonym>
        <ns2:SCDO_1000288>None</ns2:SCDO_1000288>
        <ns2:SCDO_0000303>Request inclusion into relevant ontology</ns2:SCDO_0000303>
        <ns2:IAO_0000115>Deletion of both HBA1 genes, which results in an alpha-thal-2 (alpha-/alpha-) form of alpha thalassemia trait. With this deletion there is nearly normal production of red blood cells, but there may be a mild anemia.</ns2:IAO_0000115>
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