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- NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_assertion type Assertion NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_head.
- NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_assertion wasGeneratedBy ECO_0000203 NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_provenance.
- NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_assertion wasDerivedFrom befree-20150227 NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_provenance.
- NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_assertion SIO_000772 23446743 NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_provenance.
- NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_assertion evidence source_evidence_literature NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_provenance.
- NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_assertion description "[In previous studies, we identified a loss-of-function mutation in the Cyba gene as the primary cause of hereditary eosinophilia in the Matsumoto Eosinophilia Shinshu (MES) rat strain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338791.RAPJ3hOgxAU0j1S9dUjr_LlofxD0zOvHexA6j-S-oUa54130_provenance.