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- source_evidence_literature type ECO_0000212 NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.
- NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_assertion description "[Variants located within the gene TCF7L2 are strongly associated with T2D but not with MS, providing support to previous evidence indicating that polymorphisms at the TCF7L2 gene increase T2D risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.
- NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_assertion evidence source_evidence_literature NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.
- NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_assertion SIO_000772 20503258 NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.
- NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_assertion wasDerivedFrom befree-2016 NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.
- NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_assertion wasGeneratedBy ECO_0000203 NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.
- befree-2016 importedOn "2016-02-19" NP814777.RAWno8G-JwyTD52A0mV9_yf571iOUzpOyqvaGQOKovUPE130_provenance.