Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.
- NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_assertion wasGeneratedBy ECO_0000203 NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.
- NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_assertion wasDerivedFrom befree-20150227 NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.
- NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_assertion SIO_000772 23430454 NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.
- NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_assertion evidence source_evidence_literature NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.
- NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_assertion description "[We found significant association with risk of ESCC for four SNPs, including rs1494961 in HEL308 at 4q21 [odds ratio (OR) = 1.15, 95 % confidence interval (CI) = 1.05-1.26], rs1229984 in ADH1B at 4q23 (OR = 1.24, 95 % CI = 1.13-1.36) and rs1789924 near ADH1C at 4q23 (OR = 1.20, 95 % CI = 1.03-1.39), and rs671 in ALDH2 at 12q24 (OR = 0.83, 95 % CI = 0.75-0.91).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223803.RAvwylse3bp4jV1JqWQ55Ntmc8gVowaDZ4H7YOw-mGe-s130_provenance.