Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.
- NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_assertion wasGeneratedBy ECO_0000203 NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.
- NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_assertion wasDerivedFrom befree-20140225 NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.
- NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_assertion SIO_000772 16985026 NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.
- NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_assertion evidence source_evidence_literature NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.
- NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_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." NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP895445.RAZ1xnpNQ6WWXYDp1RY6mo2FjX13N0a4ORpEzjP3jvL-E130_provenance.