Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_assertion type Assertion NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_head.
- NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_assertion description "[`Cone dystrophy with supernormal rod electroretinogram (ERG)` is an autosomal recessive disorder that causes lifelong visual loss combined with a supernormal ERG response to a bright flash of light.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.
- NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_assertion evidence source_evidence_literature NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.
- NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_assertion SIO_000772 16909397 NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.
- NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_assertion wasDerivedFrom befree-20140225 NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.
- NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_assertion wasGeneratedBy ECO_0000203 NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.