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- source_evidence_literature type ECO_0000212 NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.
- NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_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." NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.
- NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_assertion evidence source_evidence_literature NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.
- NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_assertion SIO_000772 18287869 NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.
- NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_assertion wasDerivedFrom befree-2016 NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.
- NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_assertion wasGeneratedBy ECO_0000203 NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.
- befree-2016 importedOn "2016-02-19" NP656467.RAe2ymK_fqU3oG5pPRiQrw_Z0PRdMhVD8e_oqZjegR4aM130_provenance.