Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.
- NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_assertion description "[After additional genotyping of 41 top ranked SNPs representing 24 independent signals in 5,873 individuals, combined meta-analysis revealed association of two SNPs with ESRD: rs7583877 in the AFF3 gene (P = 1.2 � 10(-8)) and an intergenic SNP on chromosome 15q26 between the genes RGMA and MCTP2, rs12437854 (P = 2.0 � 10(-9)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.
- NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_assertion evidence source_evidence_literature NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.
- NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_assertion SIO_000772 23028342 NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.
- NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_assertion wasDerivedFrom befree-2016 NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.
- NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_assertion wasGeneratedBy ECO_0000203 NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1017115.RAuElMAEhuMSawVtMU4HL-lqJw7un2e4_08mH-lOIRuxo130_provenance.