Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_assertion type Assertion NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_head.
- NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_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." NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_provenance.
- NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_assertion evidence source_evidence_literature NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_provenance.
- NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_assertion SIO_000772 21831960 NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_provenance.
- NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_assertion wasDerivedFrom befree-20140225 NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_provenance.
- NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_assertion wasGeneratedBy ECO_0000203 NP368900.RAYSJt8lWJtnwi1CSHOM2MFMeI56nYSplgfKLc0rz5PXQ130_provenance.