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- NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_assertion type Assertion NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_head.
- NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_assertion description "[We evaluated patients with hereditary retinal diseases featuring subretinal spots (retinitis punctata albescens and fundus albipunctatus) and patients with typical dominant or recessive retinitis pigmentosa for mutations in RDH5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_provenance.
- NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_assertion evidence source_evidence_literature NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_provenance.
- NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_assertion SIO_000772 10369264 NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_provenance.
- NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_assertion wasDerivedFrom befree-2016 NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_provenance.
- NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_assertion wasGeneratedBy ECO_0000203 NP255057.RA6jOltAk1SM-EQkTg7788IHyMFptlUO52BiGNFIecv0s130_provenance.