Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.
- NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_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." NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.
- NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_assertion evidence source_evidence_literature NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.
- NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_assertion SIO_000772 17463248 NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.
- NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_assertion wasDerivedFrom befree-2016 NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.
- NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_assertion wasGeneratedBy ECO_0000203 NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.
- befree-2016 importedOn "2016-02-19" NP606807.RAN1pC6yR8PK2jTjv5QSqlivGYHYolhCEbvUtqRpL1TkM130_provenance.