Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.
- NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_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." NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.
- NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_assertion evidence source_evidence_literature NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.
- NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_assertion SIO_000772 17463248 NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.
- NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_assertion wasDerivedFrom befree-20140225 NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.
- NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_assertion wasGeneratedBy ECO_0000203 NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP280549.RA5gMOQoNlSJtuq9PxHBP1yhGQ8BTeV43-PvHj3rTqheg130_provenance.