Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.
- NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_assertion description "[We genotyped 18 SNPs (r(2)<0.8 and MAF>0.05) across the region of interest: CDKN2A/B and ANRIL, encompassing the CVD-associated region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.
- NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_assertion evidence source_evidence_literature NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.
- NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_assertion SIO_000772 22178423 NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.
- NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_assertion wasDerivedFrom befree-20140225 NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.
- NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_assertion wasGeneratedBy ECO_0000203 NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP935446.RAgSbgTKCS9E75W8QjOjP2vkkWRXbrtkbcC8AnT9_GHAE130_provenance.