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- NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_assertion type Assertion NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_head.
- NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_assertion wasGeneratedBy ECO_0000203 NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_provenance.
- NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_assertion wasDerivedFrom befree-20150227 NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_provenance.
- NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_assertion SIO_000772 24222239 NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_provenance.
- NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_assertion evidence source_evidence_literature NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_provenance.
- NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_assertion description "[To determine the incidence of GATA1 mutations in a cohort of DS patients and the applicability of these mutations as a clonal marker to detect minimal residual disease, we screened 198 samples of 169 patients with DS for mutations in GATA1 exon 2 by direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418829.RAGX8OMZyfLcoFx6V2CZAMgbmuz0OAhX-nKeQMaBf83Wk130_provenance.