Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.
- NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_assertion description "[Common variations in the genes encoding C-reactive protein, tumor necrosis factor-alpha, and interleukin-6, and the risk of clinical diabetes in the Women's Health Initiative Observational Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.
- NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_assertion evidence source_evidence_literature NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.
- NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_assertion SIO_000772 21149504 NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.
- NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_assertion wasDerivedFrom befree-2016 NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.
- NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_assertion wasGeneratedBy ECO_0000203 NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.
- befree-2016 importedOn "2016-02-19" NP858357.RAbM3SnfD-T1eCC2PrsJ03pPnVB-9ktyzM__H99FwvLpI130_provenance.