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- source_evidence_literature type ECO_0000212 NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.
- NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_assertion description "[Different tests based on assessing DPD enzyme activity, genetic variants in DPYD and mRNA variants have been studied for screening for DPD deficiency, but none of these are implemented broadly into clinical practice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.
- NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_assertion evidence source_evidence_literature NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.
- NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_assertion SIO_000772 23856855 NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.
- NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_assertion wasDerivedFrom befree-2016 NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.
- NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_assertion wasGeneratedBy ECO_0000203 NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1094041.RAbsyzv0tubwN81h-pkUHFItBMJZ5SRIXZ8pbb_ctNWJQ130_provenance.