Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_assertion> ?p ?o ?g. }
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- NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_assertion type Assertion NP212787.RAD2MhGz1DWKlV39aLoid2eDjncVLOp4TR7gGH65L1xsQ130_head.
- 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.