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- NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_assertion type Assertion NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_head.
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- NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_assertion wasDerivedFrom befree-20150227 NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_provenance.
- NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_assertion SIO_000772 11875049 NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_provenance.
- NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_assertion evidence source_evidence_literature NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_provenance.
- NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_assertion description "[Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009191.RAJNI2F-ETuEr0yHU9WL1-39ah662S4FpMLst9POp5UEc130_provenance.