Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_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. In contrast, the non-synonymous ADRB3 rs4994 polymorphism is associated with T2D and MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion evidence source_evidence_literature NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion SIO_000772 20503258 NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion wasDerivedFrom gad-20130706 NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_assertion wasGeneratedBy ECO_0000203 NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49008.RAS7H6pRITFl27PHGPW85_MY3IkQ_vG8akLJxzmk84EBM130_provenance.