Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.
- NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_assertion description "[The association of apolipoprotein E (apo E) genetic polymorphism, particularly apo E2, with renal failure (plasma creatinine > or = 1.4 mg/dl, and urinary albumin excretion index > or = 300 mg/g.creatinine and/or persistent proteinuria) was investigated in 57 non-insulin-dependent diabetic (NIDDM) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.
- NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_assertion evidence source_evidence_literature NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.
- NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_assertion SIO_000772 7980694 NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.
- NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_assertion wasDerivedFrom befree-20150227 NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.
- NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_assertion wasGeneratedBy ECO_0000203 NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP233596.RAHFKkfPxyQpIAz-U4VYC6H1qwSMetgItlNorQQ8DvGAQ130_provenance.