Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.
- NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_assertion description "[As compared with genotype OO, genotypes AA and AO in females, but not in males, were associated with a significantly increased risk of GC (odds ratio [OR] 1.56 and 95 % confidence interval [CI] 1.08-2.26 for AA; OR 1.57 and 95 % CI 1.21-2.03 for AO).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.
- NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_assertion evidence source_evidence_literature NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.
- NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_assertion SIO_000772 22865192 NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.
- NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_assertion wasDerivedFrom befree-20150227 NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.
- NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_assertion wasGeneratedBy ECO_0000203 NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP991284.RAsU9GOGBIhp8mgfd5H2vTfu19xcKklFy8Qk6IR891c5Y130_provenance.