Update congenital stationary night blindness 1D

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -82836,7 +82836,7 @@ SubClassOf(obo:DOID_0110867 ObjectSomeValuesFrom(obo:RO_0004019 obo:HP_0001197))
 
 # Class: obo:DOID_0110868 (congenital stationary night blindness 1D)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/20850105") obo:IAO_0000115 obo:DOID_0110868 "A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SLC24A1 gene on chromosome 15q22.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/20850105") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/20850105/") obo:IAO_0000115 obo:DOID_0110868 "A congenital stationary night blindness characterized by a Riggs type of electroretinogram (proportionally reduced a- and b-waves) that has_material_basis_in homozygous or compound heterozygous mutation in the SLC24A1 gene on chromosome 15q22.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110868 "MIM:613830")
 AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0110868 "CSNB1D")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110868 "congenital stationary night blindness 1D autosomal recessive")