Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.
- NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_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." NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.
- NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_assertion evidence source_evidence_literature NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.
- NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_assertion SIO_000772 18461161 NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.
- NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_assertion wasDerivedFrom befree-20140225 NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.
- NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_assertion wasGeneratedBy ECO_0000203 NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP480645.RADye0iZAKBIe7sRxRuC-ETGHBlF5XMMjsyFqb437GD_c130_provenance.