Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.
- NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_assertion description "[The acquired data on single-strand breaks in DNA (SSBs), frequency of chromosomal aberrations and HPRT mutant frequency in peripheral blood lymphocytes were compared to the results on genotyping of some of the xenobiotic-metabolising enzymes (CYP1A1, CYP2E1, epoxide hydrolase and GSTM1, GSTP1 and GSTT1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.
- NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_assertion evidence source_evidence_literature NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.
- NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_assertion SIO_000772 11535253 NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.
- NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_assertion wasDerivedFrom befree-20140225 NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.
- NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_assertion wasGeneratedBy ECO_0000203 NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP531366.RAYIV8zRiCQusS1NY9rquxxzu3SDj26VQNUb8o73eIuTA130_provenance.