Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.
- NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion description "[We identify T2D-associated variants in an intergenic region of chromosome 11p12, contribute to the identification of T2D-associated variants near the genes IGF2BP2 and CDKAL1 and the region of CDKN2A and CDKN2B, and confirm that variants near TCF7L2, SLC30A8, HHEX, FTO, PPARG, and KCNJ11 are associated with T2D risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.
- NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion evidence source_evidence_literature NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.
- NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion SIO_000772 17463248 NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.
- NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion wasDerivedFrom gad-20130706 NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.
- NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion wasGeneratedBy ECO_0000203 NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance.