Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_assertion> ?p ?o ?g. }
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- NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_assertion type Assertion NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_head.
- NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_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." NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_provenance.
- NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_assertion evidence source_evidence_literature NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_provenance.
- NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_assertion SIO_000772 21822204 NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_provenance.
- NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_assertion wasDerivedFrom befree-2016 NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_provenance.
- NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_assertion wasGeneratedBy ECO_0000203 NP915255.RAUCOstGT8QVHVNnc65-6nDNhqB_JBTl4pUJHiRD21XRs130_provenance.