Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.
- NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_assertion description "[The frequencies of the T/T homozygotes were significantly higher in the patients (OR = 1.41, P = 0.013) than in the control group, confirming the association of CD14 polymorphism with MI in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.
- NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_assertion evidence source_evidence_literature NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.
- NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_assertion SIO_000772 14587643 NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.
- NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_assertion wasDerivedFrom gad-20130706 NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.
- NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_assertion wasGeneratedBy ECO_0000203 NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP47185.RAcfTgAJMVhVXORps5Y6A7HyCZSW7N8UsHe92bUx8YVTI130_provenance.