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- source_evidence_literature type ECO_0000212 NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.
- NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_assertion description "[A PCR technique was used to assay for the null genotype for GSTM1 and GSTT1 in 302 children with ALL, 57 of whom also subsequently developed treatment-related acute myeloid leukemia or myelodysplastic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.
- NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_assertion evidence source_evidence_literature NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.
- NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_assertion SIO_000772 10673738 NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.
- NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_assertion wasDerivedFrom befree-20150227 NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.
- NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_assertion wasGeneratedBy ECO_0000203 NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP441069.RAXENV792qGC9n_xss7HbLoEROIgsvvamQDg248EsyZ6c130_provenance.