Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.
- NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_assertion wasGeneratedBy ECO_0000203 NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.
- NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_assertion wasDerivedFrom befree-20150227 NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.
- NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_assertion SIO_000772 21874001 NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.
- NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_assertion evidence source_evidence_literature NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.
- NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_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 × 10(-8) to P = 1.9 × 10(-11)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841250.RA8sDFGrbbdd1ZLFKQ3qJcl8q0RPthQSoKBi4u7fTtLsw130_provenance.