Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.
- 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.
- gwascat-2016 importedOn "2016-01-27" NP51738.RAZZ0JrwUYG2hQ3veze11VIHx92w_QSJl0A2bSSnBDj0A130_provenance.