Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_assertion> ?p ?o ?g. }
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- NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_assertion type Assertion NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_head.
- 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.
- NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_assertion evidence source_evidence_literature NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_provenance.
- NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_assertion SIO_000772 25477517 NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_provenance.
- NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_assertion wasDerivedFrom befree-2016 NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_provenance.
- NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_assertion wasGeneratedBy ECO_0000203 NP1245098.RA21yFRpusGystRpftgkx81nHNs2RKTa1DqDl0KjzbQwE130_provenance.