Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_assertion evidence source_evidence_literature NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_assertion SIO_000772 10688323 NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_assertion wasDerivedFrom befree-20150227 NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_assertion wasGeneratedBy ECO_0000203 NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.