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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004022 -->

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        <rdfs:label>disease arises from feature</rdfs:label>
        <rdfs:label>disease has basis in feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0003125 -->

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        <rdfs:label>Reduced factor VIII activity</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0004841 -->

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        <rdfs:label>Reduced factor XII activity</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007595 -->

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        <rdfs:label>factor VII and Factor VIII, combined deficiency of</rdfs:label>
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        <oboInOwl:hasDbXref>OMIM:134430</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C565025</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0024565</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>factor VII and Factor VIII, combined deficiency of</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:341995</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021181 -->

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        <rdfs:label>inherited blood coagulation disorder</rdfs:label>
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