Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.
- NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_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." NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.
- NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_assertion evidence source_evidence_curated NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.
- NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_assertion SIO_000772 17463248 NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.
- NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_assertion wasDerivedFrom gwascat-2016 NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.
- NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_assertion wasGeneratedBy ECO_0000218 NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.
- gwascat-2016 importedOn "2016-01-27" NP51666.RArKAW7yQZNLgEP6oONzIAt7MUp0QxhOk2DeLt6UCiuno130_provenance.