Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP252738.RAES35FPaujAv9IukDA1iJFybHEmN9LILZPdqMDye0GwU130_provenance.