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- NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_assertion type Assertion NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_head.
- NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_assertion description "[A total of 240 different RPGR mutations have been reported, including 24 novel ones in this work, which are associated with X-linked retinitis pigmentosa (XLRP) (95%), cone, cone-rod dystrophy, or atrophic macular atrophy (3%), and syndromal retinal dystrophies with ciliary dyskinesia and hearing loss (2%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_provenance.
- NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_assertion evidence source_evidence_literature NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_provenance.
- NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_assertion SIO_000772 17195164 NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_provenance.
- NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_assertion wasDerivedFrom befree-2016 NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_provenance.
- NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_assertion wasGeneratedBy ECO_0000203 NP586496.RAbTr62Fiz-dc21if9vCIW_j_d5bhyxuwhkAobPGppgo4130_provenance.