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- source_evidence_literature type ECO_0000212 NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.
- NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion description "[Background-In long-QT syndrome (LQTS), heterozygosity for a mutation in 1 of the K(+) channel genes leads to prolongation of the cardiac action potential, because the aberrant protein exhibits loss of function. HERG, which is involved in LQT2, is the gene encoding the rapid component of the delayed rectifier, I(Kr).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.
- NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion evidence source_evidence_literature NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.
- NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion SIO_000772 10491368 NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.
- NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion wasDerivedFrom befree-2016 NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.
- NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion wasGeneratedBy ECO_0000203 NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.
- befree-2016 importedOn "2016-02-19" NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance.