Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_assertion> ?p ?o ?g. }
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- NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_assertion type Assertion NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_head.
- NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_assertion description "[Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_provenance.
- NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_assertion evidence source_evidence_literature NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_provenance.
- NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_assertion SIO_000772 18379723 NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_provenance.
- NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_assertion wasDerivedFrom befree-20140225 NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_provenance.
- NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_assertion wasGeneratedBy ECO_0000203 NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_provenance.