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- source_evidence_literature type ECO_0000212 NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.
- NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_assertion wasGeneratedBy ECO_0000203 NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.
- NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_assertion wasDerivedFrom befree-20150227 NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.
- NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_assertion SIO_000772 23342076 NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.
- NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_assertion evidence source_evidence_literature NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.
- NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_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." NP920774.RAk0d2DRiv8Qum8Ceal_daeciLRTfb0jCT7ivzC2NpS-g130_provenance.