Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.
- NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_assertion description "[Compared with the most common haplotype GGA, haplotypes AGA, GGG and GAA (each containing one variant allele) were associated with 33%, 29% and 34% significantly decreased risk of gastric cancer (adjusted OR = 0.67, 95% CI = 0.55-0.82 for AGA; OR = 0.71, 95% CI = 0.57-0.88 for GGG and OR = 0.66, 95% CI = 0.52-0.84 for GAA, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.
- NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_assertion evidence source_evidence_literature NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.
- NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_assertion SIO_000772 17433039 NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.
- NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_assertion wasDerivedFrom befree-20140225 NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.
- NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_assertion wasGeneratedBy ECO_0000203 NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP776121.RATGGBX1N6Q1G2blbWSk1HO4S0_B18-s7NnFs_6qvTUzo130_provenance.