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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

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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/11802 -->

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        <rdfs:label>TIA1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011466 -->

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        <rdfs:label>distal myopathy, Welander type</rdfs:label>
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        <ns4:IAO_0000115>Welander distal myopathy (WDM) is a distal myopathy, characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors.</ns4:IAO_0000115>
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        <oboInOwl:hasRelatedSynonym>distal myopathy, Swedish type</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>Welander distal myopathy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Welander distal myopathy, Swedish type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C0221054</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:604454</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:67441</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:603</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016108 -->

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