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- source_evidence_literature type ECO_0000212 NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.
- NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_assertion description "[A patient with ANLL FAB subtype M1 was found to possess a t(16;21)(p11;q22) and trisomy 10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.
- NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_assertion evidence source_evidence_literature NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.
- NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_assertion SIO_000772 8242597 NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.
- NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_assertion wasDerivedFrom befree-20140225 NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.
- NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_assertion wasGeneratedBy ECO_0000203 NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP655641.RANPzl4yDqqHZsRG1UjOhm5_jrYyy0hWG1QYqY6AipRGw130_provenance.