Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.
- NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_assertion description "[Heterozygous mutations in genes encoding cardiac ionic channel subunits KCNQ1, HERG, SCN5A, KCNE1, and KCNE2 are causally involved in the dominant form of long-QT syndrome (LQTS) while homozygous mutations in KCNQ1 and KCNE1 cause LQTS with or without congenital deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.
- NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_assertion evidence source_evidence_literature NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.
- NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_assertion SIO_000772 11463728 NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.
- NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_assertion wasDerivedFrom befree-20140225 NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.
- NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_assertion wasGeneratedBy ECO_0000203 NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP710189.RAvXVOCln69tyPS77SCXQiqawBXMG6a_3dtI_Vdz7DNZM130_provenance.