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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>
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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/RO_0004029 -->

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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/GO_0010669 -->

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        <rdfs:label>epithelial structure maintenance</rdfs:label>
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        <rdfs:label>Reduced circulating vitamin A concentration</rdfs:label>
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        <rdfs:label>Corneal opacity</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0001250 -->

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        <rdfs:label>keratomalacia</rdfs:label>
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        <ns4:IAO_0000115>An eye disorder that results from vitamin A deficiency, with basis in disruption of maintenance of the specialized epithelial surfaces, leading to atrophic changes in the normal mucosal surface, with loss of goblet cells, and replacement of the normal epithelium by an inappropriate keratinized stratified squamous epithelium. In addition, the substantia propria of the cornea breaks down and liquefies, resulting in keratomalacia.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>MEDGEN:57777</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>ICD9:371.45</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:85149007</oboInOwl:hasDbXref>
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        <rdfs:label>corneal degeneration</rdfs:label>
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        <rdfs:label>eye disorder</rdfs:label>
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