Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.
- NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_assertion wasGeneratedBy ECO_0000203 NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.
- NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_assertion wasDerivedFrom befree-20140225 NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.
- NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_assertion SIO_000772 10898405 NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.
- NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_assertion evidence source_evidence_literature NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.
- NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_assertion description "[It is becoming clear that mutations in the KVLQT1, human `ether-a-go-go` related gene, cardiac voltage-dependent sodium channel gene, minK and MiRP1 genes, respectively, are responsible for the LQT1, LQT2, LQT3, LQT5 and LQT6 variants of the Romano-Ward syndrome, characterized by autosomal dominant transmission and no deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP861883.RADPm0NEx9bSrq53VHnbvnxQU2n2UxabKS_ITfu1ewv0c130_provenance.