Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.
- NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_assertion description "[The numbers of cases of particular subtypes were rather small for stable estimates, but we noted that the PON1 L55M AA allele, associated with slightly increased risk of non-Hodgkin's lymphoma (variant homozygotes OR, 1.36; 95% CI, 0.96-1.95), was most strongly associated with follicular non-Hodgkin's lymphoma and T-cell lymphoma, with ORs for variant homozygotes of 2.12 and 2.93, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.
- NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_assertion evidence source_evidence_literature NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.
- NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_assertion SIO_000772 16985026 NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.
- NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_assertion wasDerivedFrom befree-2016 NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.
- NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_assertion wasGeneratedBy ECO_0000203 NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.
- befree-2016 importedOn "2016-02-19" NP570155.RAF07cSxT3PxCFlF60a3YZOXwahk05WUgu8JLo59v0WR8130_provenance.