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- NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_assertion type Assertion NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_head.
- NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_assertion description "[Mutations in human CRX are associated with the retinal diseases, cone-rod dystrophy-2 (adCRD2; refs 3, 4, 5), retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA), which all lead to loss of vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_provenance.
- NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_assertion evidence source_evidence_literature NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_provenance.
- NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_assertion SIO_000772 10581037 NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_provenance.
- NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_assertion wasDerivedFrom befree-2016 NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_provenance.
- NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_assertion wasGeneratedBy ECO_0000203 NP268761.RAAo7YNfq1MMOd5_CGRrd7CW0z7GzOJ9qZ64HxwvI5Wg4130_provenance.