Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.
- NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_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." NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.
- NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_assertion evidence source_evidence_literature NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.
- NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_assertion SIO_000772 22325160 NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.
- NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_assertion wasDerivedFrom befree-20140225 NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.
- NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_assertion wasGeneratedBy ECO_0000203 NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP838472.RAGUVUXqYlHarHFVOGebQFs2VPflDH1amPIpL9tX5tPIM130_provenance.