Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.
- NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_assertion description "[In silico follow-up analysis of putative association signals found in independent genome-wide association studies (including 8,130 cases and 38,987 controls) performed by the DIAGRAM consortium identified a T2D locus at genome-wide significance (GATAD2A/CILP2/PBX4; p = 5.7 � 10(-9)) and two loci exceeding study-wide significance (SREBF1, and TH/INS; p < 2.4 � 10(-6)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.
- NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_assertion evidence source_evidence_literature NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.
- NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_assertion SIO_000772 22325160 NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.
- NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_assertion wasDerivedFrom befree-2016 NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.
- NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_assertion wasGeneratedBy ECO_0000203 NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.
- befree-2016 importedOn "2016-02-19" NP960077.RAgjMrg8dcM5RL_kot0yFQpqcmgFcW0ilq4rukZgLgsLc130_provenance.