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- source_evidence_literature type ECO_0000212 NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion description "[Subgroup analysis showed that the presence of the K897T polymorphism in the LQT2 gene in an affected family was associated with an 11-fold (P=0.001) increase in the risk of recurrent syncope in genotype-negative subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion evidence source_evidence_literature NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion SIO_000772 21831960 NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion wasDerivedFrom befree-2016 NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion wasGeneratedBy ECO_0000203 NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- befree-2016 importedOn "2016-02-19" NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.