Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.
- NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_assertion description "[In addition to TCF7L2, SLC30A8 and HHEX, initially identified by the French GWA scan, CDKAL1, IGFBP2 and CDKN2A/2B strongly associate with T2D in French individuals, and mostly in populations of Central European descent but not in Moroccan subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.
- NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_assertion evidence source_evidence_literature NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.
- NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_assertion SIO_000772 18461161 NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.
- NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_assertion wasDerivedFrom befree-2016 NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.
- NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_assertion wasGeneratedBy ECO_0000203 NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.
- befree-2016 importedOn "2016-02-19" NP669598.RAMiAxwAbHzzYu6pJR95Ii2mJYEYLPS4K56KBgyKtLUdY130_provenance.