Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_assertion> ?p ?o ?g. }
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- NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_assertion type Assertion NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_head.
- NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_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." NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_provenance.
- NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_assertion evidence source_evidence_literature NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_provenance.
- NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_assertion SIO_000772 20503258 NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_provenance.
- NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_assertion wasDerivedFrom befree-2016 NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_provenance.
- NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_assertion wasGeneratedBy ECO_0000203 NP814771.RArX_51XkhluFxZiWKus9KkEJnyEFRfQ1fABOG65Nnng4130_provenance.