Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.
- NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_assertion description "[We have shown for the first time that variants at WFS1, JAZF1, SLC30A8, CDKN2A/B, TCF7L2, KCNQ1, HMG20A, HNF4A and DUSP9 are associated with T2D in the Saudi population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.
- NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_assertion evidence source_evidence_literature NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.
- NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_assertion SIO_000772 23448427 NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.
- NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_assertion wasDerivedFrom befree-20150227 NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.
- NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_assertion wasGeneratedBy ECO_0000203 NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP461294.RAqOC5FATOZ1dv_nG_OTt6iSe5thQxyptFuEUOjNKY-eM130_provenance.