Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_assertion> ?p ?o ?g. }
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- NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_assertion type Assertion NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_head.
- NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_assertion description "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_provenance.
- NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_assertion evidence source_evidence_literature NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_provenance.
- NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_assertion SIO_000772 10704189 NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_provenance.
- NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_assertion wasDerivedFrom befree-2016 NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_provenance.
- NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_assertion wasGeneratedBy ECO_0000203 NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_provenance.