Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_assertion> ?p ?o ?g. }
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- NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_assertion type Assertion NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_head.
- NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_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." NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.
- NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_assertion evidence source_evidence_literature NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.
- NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_assertion SIO_000772 10369264 NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.
- NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_assertion wasDerivedFrom befree-20140225 NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.
- NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_assertion wasGeneratedBy ECO_0000203 NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.