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- NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_assertion type Assertion NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_head.
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- NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_assertion wasDerivedFrom befree-20140225 NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_provenance.
- NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_assertion SIO_000772 16272056 NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_provenance.
- NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_assertion evidence source_evidence_literature NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_provenance.
- NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_assertion description "[Aiming towards an understanding of the molecular background of retinitis pigmentosa, this paper describes the phenotype of a Swedish family with a mutation in IMPDH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858563.RAAWJl_C8h6cmtrQnZPSqe1HiZW4j4wC0yx3WvBzH0woU130_provenance.