Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.
- NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_assertion description "[Genotyping analysis demonstrated that 2 SNPs among 13 were significantly associated with ESRD after adjusting for age and sex, which were shown by IL17E rs10137082 (odds ratio (OR) 1.48 in codominant 1, OR 1.54 in dominant, OR 1.47 in log-additive) and IL17RA rs4819554 (OR 1.46 in codominant 1, OR 1.79 in codominant 2, OR 1.54 in dominant, OR 1.39 in log-additive).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.
- NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_assertion evidence source_evidence_literature NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.
- NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_assertion SIO_000772 23147652 NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.
- NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_assertion wasDerivedFrom befree-20150227 NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.
- NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_assertion wasGeneratedBy ECO_0000203 NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP882655.RAaNZ0eBaFH1PhnB0javXPm0O-rX5wdvh_95tE9BYdzIU130_provenance.