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- source_evidence_literature type ECO_0000212 NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.
- NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_assertion description "[Even with the most conservative Bonferroni adjustment, two 2-SNP-haplotypes in SLC41A2 and MRS2 region were significantly associated with T2D risk (rs12582312-rs10861279: P = 0.0006; rs1056285-rs7738943: P = 0.002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.
- NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_assertion evidence source_evidence_literature NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.
- NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_assertion SIO_000772 25733456 NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.
- NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_assertion wasDerivedFrom befree-2016 NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.
- NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_assertion wasGeneratedBy ECO_0000203 NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267648.RANou_yeFrH_pq3FH0YPbWOoX0l4FkNMLH2O9I9nevZUA130_provenance.