Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.
- NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_assertion description "[The occurrence of null alleles, the inclusion of T2D patients in analyses of metabolic syndrome risk traits and the genetic model, are possible factors accounting for non-replications of IGF2BP2 associations with T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.
- NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_assertion evidence source_evidence_literature NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.
- NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_assertion SIO_000772 20627640 NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.
- NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_assertion wasDerivedFrom gad-20150221 NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.
- NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_assertion wasGeneratedBy ECO_0000203 NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP84300.RA0TWG1IGWsgHEoTZF4JCz56DkCZX--oF8hnYEyf96GI4130_provenance.