Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.
- NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_assertion description "[In a discovery cohort of 1804 melanoma cases and 1026 controls, we identified loci at chromosomes 15q13.1 (HERC2/OCA2 region) and 16q24.3 (MC1R) regions that reached genome-wide significance within this study and also found strong evidence for genetic effects on susceptibility to melanoma from markers on chromosome 9p21.3 in the p16/ARF region and on chromosome 1q21.3 (ARNT/LASS2/ANXA9 region).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.
- NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_assertion evidence source_evidence_literature NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.
- NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_assertion SIO_000772 21926416 NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.
- NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_assertion wasDerivedFrom befree-20140225 NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.
- NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_assertion wasGeneratedBy ECO_0000203 NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP865769.RAAddGgpkH7k8apo4VzsDbDoNW0adh1EqOg4E_VaQtPqs130_provenance.