Matches in Nanopublications for { ?s ?p "[LCA1 is a severe form of retinal dystrophy caused by loss-of-function mutations in guanylate cyclase 1 (GC1), a key member of the phototransduction cascade involved in modulating the photocurrents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[LCA1 is a severe form of retinal dystrophy caused by loss-of-function mutations in guanylate cyclase 1 (GC1), a key member of the phototransduction cascade involved in modulating the photocurrents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_assertion description "[LCA1 is a severe form of retinal dystrophy caused by loss-of-function mutations in guanylate cyclase 1 (GC1), a key member of the phototransduction cascade involved in modulating the photocurrents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_provenance.