Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_assertion> ?p ?o ?g. }
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- NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_assertion type Assertion NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_head.
- NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_assertion description "[Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause `cone dystrophy with supernormal rod electroretinogram` in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.
- NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_assertion evidence source_evidence_literature NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.
- NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_assertion SIO_000772 16909397 NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.
- NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_assertion wasDerivedFrom befree-20140225 NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.
- NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_assertion wasGeneratedBy ECO_0000203 NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.