Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_assertion type Assertion NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_head.
- NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_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." NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_provenance.
- NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_assertion evidence source_evidence_literature NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_provenance.
- NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_assertion SIO_000772 10369264 NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_provenance.
- NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_assertion wasDerivedFrom befree-20150227 NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_provenance.
- NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_assertion wasGeneratedBy ECO_0000203 NP668520.RAdfGx76V2YbZ90krsOvBUjTa8dtu7nLcRIQkUiS8vZco130_provenance.