Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_assertion type Assertion NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_head.
- NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_assertion description "[Mutations of the gap junction beta 2 (GJB2) gene coding for the protein connexin 26 account for up to 50% of nonsyndromic sensorineural hearing loss (NSHL), with specific mutations associated with distinct ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_provenance.
- NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_assertion evidence source_evidence_literature NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_provenance.
- NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_assertion SIO_000772 12169891 NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_provenance.
- NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_assertion wasDerivedFrom befree-20140225 NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_provenance.
- NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_assertion wasGeneratedBy ECO_0000203 NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_provenance.