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- source_evidence_literature type ECO_0000212 NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion description "[Independent risk factors for syncope in genotype-negative subjects included female sex (hazard ratio [HR], 1.60; P=0.002), prolonged QTc (HR=1.63 per 100 ms increment, P=0.02), family history of ACA or SCD (HR=1.89, P=0.002), and LQT2 versus LQT1 family mutation (HR=1.41, P=0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion evidence source_evidence_literature NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion SIO_000772 21831960 NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion wasDerivedFrom befree-20140225 NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion wasGeneratedBy ECO_0000203 NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- befree-20140225 importedOn "2014-02-25" NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.