Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.
- NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_assertion description "[Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.
- NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_assertion evidence source_evidence_literature NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.
- NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_assertion SIO_000772 20571754 NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.
- NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_assertion wasDerivedFrom gad-20130706 NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.
- NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_assertion wasGeneratedBy ECO_0000203 NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP77890.RA1fjgLL9oXATe0bRZs33lisItMP5K0IpS5WMKBNAg3hI130_provenance.