Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.
- NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_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." NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.
- NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_assertion evidence source_evidence_curated NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.
- NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_assertion SIO_000772 17463248 NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.
- NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_assertion wasDerivedFrom gwascat-2016 NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.
- NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_assertion wasGeneratedBy ECO_0000218 NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.
- gwascat-2016 importedOn "2016-01-27" NP51664.RAcrfGfMq2qnBKM1P4gbV1HxDdYxx8yBYkbsDy3lossNk130_provenance.