Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.
- NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_assertion description "[Subjects who were heterozygous or homozygous for the cytochrome P450 gene variant CYP1B1 V432L G allele were at slightly greater risk of non-Hodgkin's lymphoma [odds ratio (OR), 1.27; 95% confidence interval (95% CI), 0.97-1.65]; these results were consistent across B-cell lymphoma subtypes and among both non-Hispanic White and Black subjects, although not statistically significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.
- NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_assertion evidence source_evidence_literature NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.
- NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_assertion SIO_000772 16985026 NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.
- NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_assertion wasDerivedFrom befree-2016 NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.
- NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_assertion wasGeneratedBy ECO_0000203 NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.
- befree-2016 importedOn "2016-02-19" NP570159.RADDqww88h9USKHRS4MpqxWF-H5_UwR6UXZdInQoOc8iE130_provenance.