Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.
- NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_assertion description "[In the population studied, persons with glutathione-S-transferase M1 null genotype and N-acetyl transferase 2*6B allele are at increased risk of developing AML, and the risk is considerably enhanced in persons with both glutathione-S-transferase M1 and N-acetyl transferase 2 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.
- NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_assertion evidence source_evidence_literature NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.
- NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_assertion SIO_000772 18287869 NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.
- NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_assertion wasDerivedFrom gad-20130706 NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.
- NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_assertion wasGeneratedBy ECO_0000203 NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP43114.RAlx9RZIA3AHnOnN1w2LInER_bPInsXK5Yk3PJcWLHBUI130_provenance.