Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_assertion> ?p ?o ?g. }
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- NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_assertion type Assertion NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_head.
- NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_provenance.
- NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_assertion evidence source_evidence_literature NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_provenance.
- NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_assertion SIO_000772 10581037 NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_provenance.
- NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_assertion wasDerivedFrom befree-2016 NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_provenance.
- NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_assertion wasGeneratedBy ECO_0000203 NP268763.RAgQX3ejLZ6OR5lrhH3p5pe3h1Ar9_yHTNrtX66BIUOQk130_provenance.