Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion> ?p ?o ?g. }
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- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion type Assertion NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_head.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion wasGeneratedBy ECO_0000203 NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion wasDerivedFrom befree-20140225 NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion SIO_000772 21831960 NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_provenance.
- NP621601.RAPd7yFVnelTd7BSESvfOsg4ior8M-wjBtsg6a69gfX34130_assertion evidence source_evidence_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.