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- source_evidence_literature type ECO_0000212 NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_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." NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_assertion evidence source_evidence_literature NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_assertion SIO_000772 10688323 NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_assertion wasDerivedFrom befree-2016 NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_assertion wasGeneratedBy ECO_0000203 NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- befree-2016 importedOn "2016-02-19" NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.