Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.
- NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_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." NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.
- NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_assertion evidence source_evidence_literature NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.
- NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_assertion SIO_000772 7980694 NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.
- NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_assertion wasDerivedFrom befree-2016 NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.
- NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_assertion wasGeneratedBy ECO_0000203 NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1328946.RA69j1gKcj4So9Ir9z3bHeBSZzlYD8iGhdrf64YqYaw-w130_provenance.