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- NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_assertion type Assertion NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_head.
- NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_assertion description "[An inosine monophosphate dehydrogenase 1 (IMPDH1) pseudogene carries a c.676G>A mutation that produces a p.Asp226Asn substitution that causes the retinitis pigmentosa 10 (RP10) form of adRP; and a phosphoglycerate kinase 1 (PGK1) pseudogene (PGK1P1) carries a c.837T>C mutation that produces a p.Ile252Thr substitution that is associated with a phosphoglycerate kinase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_provenance.
- NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_assertion evidence source_evidence_literature NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_provenance.
- NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_assertion SIO_000772 16671097 NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_provenance.
- NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_assertion wasDerivedFrom befree-20150227 NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_provenance.
- NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_assertion wasGeneratedBy ECO_0000203 NP509556.RAKstsXFOavEd9-ZfoMB_iUIV3TXuwzPNIauSvm67c02g130_provenance.