Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_assertion> ?p ?o ?g. }
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- NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_assertion type Assertion NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_head.
- NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_assertion description "[When a stringent statistical correction for multiple testing was used, the only significant SNP was at TCF7L2, which has already been discovered and confirmed as a T2D-susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.
- NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_assertion evidence source_evidence_curated NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.
- NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_assertion SIO_000772 17668382 NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.
- NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_assertion wasDerivedFrom gwascat-2016 NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.
- NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_assertion wasGeneratedBy ECO_0000218 NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.