Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion> ?p ?o ?g. }
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- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion type Assertion NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_head.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion wasGeneratedBy ECO_0000203 NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion wasDerivedFrom befree-2016 NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion SIO_000772 19878917 NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion evidence source_evidence_literature NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.
- NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP772891.RACJph_lGAw_Ip-dDIYtdzcCLTdaCxY1AmqDjgi7ScOgI130_provenance.