Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.
- NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_assertion wasGeneratedBy ECO_0000218 NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.
- NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_assertion wasDerivedFrom ctd_human-20150221 NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.
- NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_assertion SIO_000772 21874001 NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.
- NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_assertion evidence source_evidence_curated NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.
- NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_assertion description "[In the combined analysis, we identified common genetic variants at six loci (GRB14, ST6GAL1, VPS26A, HMG20A, AP3S2 and HNF4A) newly associated with T2D (P = 4.1 A 10(-8) to P = 1.9 A 10(-11)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP16256.RAJwq8GXBWT9ssRBr6FOBGbPbTFvtzNFMfQAABva5f9r8130_provenance.