Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.
- NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_assertion description "[The CYP1B1 V432L homozygous variant was associated with decreased risk of meningioma (odds ratio [OR] = 0.6; 95% CI, 0.3-1.0) but not the other tumor types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.
- NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_assertion evidence source_evidence_literature NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.
- NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_assertion SIO_000772 16598069 NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.
- NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_assertion wasDerivedFrom befree-20150227 NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.
- NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_assertion wasGeneratedBy ECO_0000203 NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP340275.RAmM8mjkU4BUzb6W5wrtgklDS53_1tESUnKxcIvlispgs130_provenance.