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- source_evidence_literature type ECO_0000212 NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.
- NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_assertion description "[In this study we analyzed bone marrow and blood samples from 13 patients with myeloid leukemia (de novo myelodysplastic syndrome [MDS], n = 3; de novo acute myeloid leukemia [AML], n = 9; therapy-related (t-) AML, n = 1) which, on chromosome banding analysis, exhibited deletions (n = 12) or in one case a balanced translocation involving bands 7q31-qter using fluorescence in situ hybridization (FISH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.
- NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_assertion evidence source_evidence_literature NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.
- NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_assertion SIO_000772 9834205 NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.
- NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_assertion wasDerivedFrom befree-20150227 NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.
- NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_assertion wasGeneratedBy ECO_0000203 NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781387.RAUIL0ODwrwL7Y9pOASErX4XdFgTLrw4T_oS0jkEQ4kJA130_provenance.