Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_assertion> ?p ?o ?g. }
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- NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_assertion type Assertion NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_head.
- NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_assertion description "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_provenance.
- NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_assertion evidence source_evidence_literature NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_provenance.
- NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_assertion SIO_000772 19426954 NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_provenance.
- NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_assertion wasDerivedFrom befree-20140225 NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_provenance.
- NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_assertion wasGeneratedBy ECO_0000203 NP296779.RA3iNGJxAmy5FTPBGODypg1MzUCxmTZ9cBHHh7Ze6YMEM130_provenance.