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- source_evidence_literature type ECO_0000212 NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_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." NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_assertion evidence source_evidence_literature NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_assertion SIO_000772 10688323 NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_assertion wasDerivedFrom befree-20150227 NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_assertion wasGeneratedBy ECO_0000203 NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.