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- source_evidence_literature type ECO_0000212 NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.
- NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_assertion wasGeneratedBy ECO_0000203 NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.
- NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_assertion wasDerivedFrom befree-20150227 NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.
- NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_assertion SIO_000772 15901999 NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.
- NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_assertion evidence source_evidence_literature NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.
- NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_assertion description "[The GST T1 null genotype frequency in CML patients is significantly different from that in controls (odds ratio (OR) 3.12, 95% confidence interval (CI) 1.3-7.45, P=0.008).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP971370.RABi26ThhdOR3NIO33MLJYN40hBXwxHLVyFDypnzg330c130_provenance.