Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.
- NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_assertion wasGeneratedBy ECO_0000203 NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.
- NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_assertion wasDerivedFrom befree-2016 NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.
- NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_assertion SIO_000772 25066213 NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.
- NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_assertion evidence source_evidence_literature NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.
- NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_assertion description "[Although no other associations were significant after multiple testing correction, variants in SHMT1 in 1-C transfer, previously reported with OC, suggested lower risk at higher folate (p(interaction) = 0.03-0.006).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1205386.RAeOxlPuj0lIG8GEv-r3yeV2O2k-eJK875o7knU0DnhQ0130_provenance.