Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.
- NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_assertion description "[MTHFR C677T [OR: 1.96, 95% CI: 1.06-3.61] and GCP II C1561T [OR: 2.09, 95% CI: 1.09-3.97] were found to be associated with risk for CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.
- NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_assertion evidence source_evidence_literature NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.
- NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_assertion SIO_000772 19394322 NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.
- NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_assertion wasDerivedFrom befree-20140225 NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.
- NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_assertion wasGeneratedBy ECO_0000203 NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP630589.RAKTzAfGdjhLQMHYgeeOBdeICvTwoP9RkeIxyD2TB2w1Q130_provenance.