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- source_evidence_literature type ECO_0000212 NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP763486.RAeyw2mIgLQo7M2rY-LQ7P9sNMX34xcU_IgEUyldWM_RM130_provenance.