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- source_evidence_literature type ECO_0000212 NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.
- NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_assertion description "[We report two cases of AML who presented with well-characterised cytogenetic abnormalities at presentation: t(8;21) and t(15;17) respectively, and who, after achieving complete morphological and cytogenetic remissions post-autograft, developed MDS/AML associated with monosomy 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.
- NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_assertion evidence source_evidence_literature NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.
- NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_assertion SIO_000772 9603416 NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.
- NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_assertion wasDerivedFrom befree-20150227 NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.
- NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_assertion wasGeneratedBy ECO_0000203 NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978517.RAAup3SmXq-lux492DgVi0P62rVmc7sOvppvLAQuD3c6o130_provenance.