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- NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_assertion type Assertion NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_head.
- NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_assertion wasGeneratedBy ECO_0000203 NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_provenance.
- NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_assertion wasDerivedFrom befree-2016 NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_provenance.
- NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_assertion SIO_000772 23751892 NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_provenance.
- NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_assertion evidence source_evidence_literature NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_provenance.
- NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_assertion description "[This is the first report on an 8p11 MPN with a trisomy 21 RUNX1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1084627.RACVn0-Vzpv48gB0VXjSzPWk9US9ZdfXIMO9f3f_GDsJM130_provenance.