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- NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_assertion type Assertion NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_head.
- NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_assertion description "[Here we demonstrate that runx1 deletion in mice induces the persistence of MYH10 in platelets, and a similar persistence was observed in platelets of patients with constitutional (familial platelet disorder/acute myeloid leukemia) or acquired (chronic myelomonocytic leukemia) RUNX1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_provenance.
- NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_assertion evidence source_evidence_literature NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_provenance.
- NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_assertion SIO_000772 22677128 NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_provenance.
- NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_assertion wasDerivedFrom befree-2016 NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_provenance.
- NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_assertion wasGeneratedBy ECO_0000203 NP988092.RA3peePVKM_0datXqF53A_TnsL9IO4hisQomLFsrAjZO0130_provenance.