Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_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." NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_assertion evidence source_evidence_literature NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_assertion SIO_000772 10688323 NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_assertion wasDerivedFrom befree-2016 NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_assertion wasGeneratedBy ECO_0000203 NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- befree-2016 importedOn "2016-02-19" NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.