Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_assertion description "[Mutations in CACNA1C that increase current through the CaV1.2 L-type Ca2+ channel underlie rare forms of long QT syndrome (LQTS), and Timothy syndrome (TS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_assertion evidence source_evidence_literature NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_assertion SIO_000772 25184293 NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_assertion wasDerivedFrom befree-2016 NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_assertion wasGeneratedBy ECO_0000203 NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.