Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.
- NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_assertion description "[When evaluating the risk of COMT polymorphisms with stage or grade of cancer, no associations were observed for any of the genotypes with the exception of a tendency (P = 0.096) for the variant A allele on codon 158 to be correlated with higher stages (> or = T3) of cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.
- NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_assertion evidence source_evidence_literature NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.
- NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_assertion SIO_000772 16492910 NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.
- NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_assertion wasDerivedFrom befree-20140225 NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.
- NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_assertion wasGeneratedBy ECO_0000203 NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_provenance.