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- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion type Assertion NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_head.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion wasGeneratedBy ECO_0000218 NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion wasDerivedFrom ctd_human-20150221 NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion SIO_000772 16384941 NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion evidence source_evidence_curated NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.
- NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19455.RAUCcO_Yew5KbHn07M24UfouhtDJFrqv-b9_vWj4Y0VmQ130_provenance.