Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.
- NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_assertion description "[We compared cadherin 23 (Cdh23) mRNA and protein variants in the inner ear and retina of wild-type and mutant mice and primates to better understand the pleiotropic effects of Cdh23 mutations, and specifically to understand the absence of retinal degeneration in Cdh23 mutant mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.
- NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_assertion evidence source_evidence_literature NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.
- NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_assertion SIO_000772 19756182 NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.
- NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_assertion wasDerivedFrom befree-20140225 NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.
- NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_assertion wasGeneratedBy ECO_0000203 NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718708.RA25Vaw7m4dtqVPKRguYH1Ma51MRTunmKln4e6LdiU26k130_provenance.