Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.
- NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_assertion description "[However, there is no evidence that APOA5 S19W, -12,238T > C, APOA4 T347S and APCC3 -482C > T SNPs are major risk factors of CHD in French men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.
- NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_assertion evidence source_evidence_literature NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.
- NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_assertion SIO_000772 16321685 NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.
- NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_assertion wasDerivedFrom befree-20140225 NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.
- NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_assertion wasGeneratedBy ECO_0000203 NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP618935.RARKjMxA5p8U4UL4s9ghOuCytQ2Onhze8Sg46cqFudoLg130_provenance.