Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_assertion> ?p ?o ?g. }
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- NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_assertion type Assertion NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_head.
- NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_assertion description "[Recurrent genetic abnormalities in B-lymphoblastic leukemia with prognostic significance are well known and specifically delineated in the WHO 2008 classification (eg hyperdiploidy, t(9;22)(q34;q11.2); BCR-ABL1, t(12;21)(p13;q22); ETV6-RUNX1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_provenance.
- NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_assertion evidence source_evidence_literature NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_provenance.
- NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_assertion SIO_000772 21822204 NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_provenance.
- NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_assertion wasDerivedFrom befree-20150227 NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_provenance.
- NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_assertion wasGeneratedBy ECO_0000203 NP265487.RAXi0HIT8BelrhQrlYZQjoBr6V_yWPMNekGSRaUZl4MYE130_provenance.