Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.
- NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_assertion description "[In the patients with RA and amyloidosis, those with nephropathy had significantly higher TNFalpha and sTNFRI levels than did those without nephropathy; in patients with isolated proteinuria (but no creatinine elevation) the TNFalpha level was also significantly increased, indicating that the TNFalpha elevation was not merely a consequence of impaired renal function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.
- NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_assertion evidence source_evidence_literature NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.
- NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_assertion SIO_000772 14613268 NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.
- NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_assertion wasDerivedFrom befree-20140225 NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.
- NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_assertion wasGeneratedBy ECO_0000203 NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP818197.RAIQA5wsqwYB9naL4MOpSHIqBClWBQ3rCB_XV2vQ4Pjp4130_provenance.