Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.
- NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_assertion description "[However, in the presence of at least a single copy of the variant CYP1A1 MspI allele and the CYP2D6 HEM genotype, the risk was two-fold for squamous cell carcinoma (SQCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.
- NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_assertion evidence source_evidence_literature NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.
- NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_assertion SIO_000772 14602525 NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.
- NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_assertion wasDerivedFrom befree-20140225 NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.
- NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_assertion wasGeneratedBy ECO_0000203 NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.
- befree-20140225 importedOn "2014-02-25" NP637845.RABFUxjCyw1B15E5qjKc3p1YVuwDEUk_z53DRescMbJic130_provenance.