Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.
- befree-2016 importedOn "2016-02-19" NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.
- NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_assertion wasGeneratedBy ECO_0000203 NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.
- NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_assertion wasDerivedFrom befree-2016 NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.
- NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_assertion SIO_000772 15120704 NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.
- NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_assertion evidence source_evidence_literature NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.
- NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_assertion description "[To test this hypothesis we searched for association between the A-->G (-3862) variant in UCP1, the insertion/deletion (I/D) polymorphism in exon 8 in UCP2, and the C-->T (-55) polymorphism in UCP3 and diabetic nephropathy in 218 diabetic patients with normal urinary albumin excretion rate (AER), 216 with micro- or macroalbuminuria, and in 106 control subjects without a family history of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442272.RATl-llCRNWaz9fRL7NAe3HkLTq74FJEOq4-RcTTm6zjk130_provenance.