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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/443 -->

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        <rdfs:label>ALS2</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005144 -->

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        <rdfs:label>familial amyotrophic lateral sclerosis</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C1859807</oboInOwl:hasDbXref>
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        <rdfs:label>juvenile amyotrophic lateral sclerosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100227 -->

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        <rdfs:label>ALS2-related motor neuron disease</rdfs:label>
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