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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/4315 -->

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        <rdfs:label>GLE1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0012750 -->

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        <rdfs:label>lethal arthrogryposis-anterior horn cell disease syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>OMIM:611890</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:1677784</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>LAAHD</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>congenital arthrogryposis with anterior horn cell disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:53696</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Vuopala disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0016658</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C567502</oboInOwl:hasDbXref>
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        <rdfs:label>arthrogryposis multiplex congenita</rdfs:label>
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