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- source_evidence_literature type ECO_0000212 NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.
- NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_assertion wasGeneratedBy ECO_0000203 NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.
- NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_assertion wasDerivedFrom befree-20150227 NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.
- NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_assertion SIO_000772 15193435 NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.
- NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_assertion evidence source_evidence_literature NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.
- NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_assertion description "[The genetic changes with especially large discrepancy rates at diagnosis were del(7q) (20.0%), PML/RARA (17.6%), and trisomy 21 (12.5%) and, at follow-up, BCR/ABL (28.2%) and AML1/ETO (24.4%); the latter two showed only small discrepancies at diagnosis (4.7 and 4.8%, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285530.RAAhwhaQolkA0OUT2AJjsAHiCqj5bn-i-DhsO_TyQcd3M130_provenance.