Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_assertion> ?p ?o ?g. }
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- NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_assertion type Assertion NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_head.
- NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_assertion description "[Among 18 BCR-ABL+ leukemias presenting acquired trisomy of chromosome 21, we report a high frequency (33%) of recurrent point mutations (4 in myeloid blast crisis [BC] CML and one in chronic phase CML) within the DNA-binding region of RUNX1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_provenance.
- NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_assertion evidence source_evidence_literature NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_provenance.
- NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_assertion SIO_000772 18202228 NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_provenance.
- NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_assertion wasDerivedFrom befree-2016 NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_provenance.
- NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_assertion wasGeneratedBy ECO_0000203 NP650496.RAA3FU5C4d2e0Z8hUJXouXG6-MTna0esg1VoNUpBdqcvI130_provenance.