Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.
- NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_assertion description "[Genotype combinations characterized by the presence of two variant genotypes on their corresponding loci revealed that four combinations of GSTT1 null and MnSOD(-9Val) or GST null and MAOB-G or CYP2E1*5B and MAO-B-AG or CYP2E1*5B and DRD2 (Taq1A-het) genotypes in the patients exhibited severalfold higher and significant association with risk to PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.
- NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_assertion evidence source_evidence_literature NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.
- NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_assertion SIO_000772 18327668 NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.
- NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_assertion wasDerivedFrom befree-20140225 NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.
- NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_assertion wasGeneratedBy ECO_0000203 NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP248214.RAZtmG13K08q0VjFjgQ2GNx2grnFoomh5Hi94GFjO4vQA130_provenance.