Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.
- NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_assertion wasGeneratedBy ECO_0000203 NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.
- NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_assertion wasDerivedFrom befree-20150227 NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.
- NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_assertion SIO_000772 23342076 NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.
- NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_assertion evidence source_evidence_literature NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.
- NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_assertion description "[We genotyped a leucine repeat polymorphism (D18S880) that is within CNDP1 along with 29 single nucleotide polymorphisms (SNPs) in the CNDP1/CNDP2 locus for 2,740 Japanese subjects with type 2 diabetes (1,205 nephropathy cases with overt nephropathy or with end-stage renal disease [ESRD], and 1,535 controls with normoalbuminuria).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920768.RAIntZ7sn08YL17GCrUExJAsmy2EMTfLiqDRbAAl8IPSc130_provenance.