Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.
- NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_assertion description "[In all 271 patients (irrespective of age) with normal arteries, the frequency of factor V Leiden was 11.7% (7/60) compared with 4.3% (9/211) in patients with at least one >50% stenosis (OR 2.9 [95% CI 1.1-8.3], p = 0.04), and the frequency of prothrombin variant G20210A was 6.7% (4/60) compared with 1.4% (3/211) (OR 4.9 [95% CI 1.1-22.8], p = 0.04), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.
- NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_assertion evidence source_evidence_literature NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.
- NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_assertion SIO_000772 10987590 NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.
- NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_assertion wasDerivedFrom befree-20140225 NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.
- NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_assertion wasGeneratedBy ECO_0000203 NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP586366.RAwFbrRGcCQG8LUta8oGIs3xE-DP8lTx9Nb6JDTvu5tBw130_provenance.