Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP476721.RACMrgQTA7SgtMc7qhhwuuQHHk18TBZYX451v1fLKbYT8130_provenance.