Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_assertion> ?p ?o ?g. }
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- NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_assertion type Assertion NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_head.
- NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_assertion description "[Incomplete X-linked congenital stationary night blindness (CSNB) is a clinically variable condition that has been shown to be caused by mutations in the calcium-channel CACNA1F gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_provenance.
- NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_assertion evidence source_evidence_literature NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_provenance.
- NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_assertion SIO_000772 10900517 NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_provenance.
- NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_assertion wasDerivedFrom befree-20140225 NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_provenance.
- NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_assertion wasGeneratedBy ECO_0000203 NP563811.RAKuHdqJKNvZLR2G5N8PUkGdT1YTM5dPry1A9TGnwMbIo130_provenance.