Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.
- NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_assertion wasGeneratedBy ECO_0000203 NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.
- NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_assertion wasDerivedFrom befree-20150227 NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.
- NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_assertion SIO_000772 19720796 NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.
- NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_assertion evidence source_evidence_literature NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.
- NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_assertion description "[However, in multivariable Cox models, an approximately twofold increased risk was observed for the Hp 2/2 compared with the Hp 1/1 genotype for eGFR decline (hazard ratio 1.79 [95% CI 1.06-3.00]) and ESRD (2.74 [1.17-6.45]); no significant associations were observed for microalbuminuria or macroalbuminuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983682.RAeVp6lSYgqZtux0CyjtvnDJPd6mbTzkVieTb7MPv1vcs130_provenance.