Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.
- NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_assertion description "[In European Americans, variants within C-reactive protein (CRP) and glial cell line-derived neurotrophic factor (GDNF) were associated with AHI (CRP: = 4.6; SE = 1.1; P = 0.0000402) (GDNF: = 4.3; SE = 1; P = 0.0000201) and with the dichotomous OSA trait (CRP: odds ratio = 2.4; 95% confidence interval, 1.5-3.9; P = 0.000170) (GDNF: odds ratio = 2; 95% confidence interval, 1.4-2.89; P = 0.0000433).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.
- NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_assertion evidence source_evidence_literature NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.
- NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_assertion SIO_000772 20538960 NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.
- NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_assertion wasDerivedFrom gad-20130706 NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.
- NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_assertion wasGeneratedBy ECO_0000203 NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP89182.RAWqvFCTpwQty4TmEm_lc1dc1BZlpyYCFd5s8JBruSXzE130_provenance.