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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/11590 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0011627 -->

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        <ns4:IAO_0000115>A neurodevelopmental disorder caused by the mutation in the TBR1 gene and characterized by varying degrees of intellectual disability, autism spectrum disorder, and language deficits.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>MEDGEN:340048</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020836 -->

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