Fix label/synonym issues

Author: allenbaron

src/ontology/doid-edit.owl

@@ -34044,7 +34044,6 @@ AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060346 "UMLS_CUI:C1850625")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0060346 "Bailey-Bloch congenital myopathy")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0060346 "Native American myopathy")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0060346 "STAC3 disorder")
-AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0060346 "congenital myopathy 13")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0060346 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0060346 "DOID:0060346")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0060346 doid:DO_rare_slim)
@@ -38254,15 +38253,15 @@ AnnotationAssertion(oboInOwl:inSubset obo:DOID_0060671 doid:DO_rare_slim)
 AnnotationAssertion(rdfs:label obo:DOID_0060671 "cerebral cavernous malformation 3")
 SubClassOf(obo:DOID_0060671 obo:DOID_0060669)
 
-# Class: obo:DOID_0060672 (Grn-related frontotemporal lobar degeneration with Tdp43 inclusions)
+# Class: obo:DOID_0060672 (GRN-related frontotemporal lobar degeneration with Tdp43 inclusions)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/16862116") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/16983677") obo:IAO_0000115 obo:DOID_0060672 "A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060672 "ICD10CM:G31.0")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060672 "MIM:607485")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0060672 "frontotemporal dementia 2")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0060672 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0060672 "DOID:0060672")
-AnnotationAssertion(rdfs:label obo:DOID_0060672 "Grn-related frontotemporal lobar degeneration with Tdp43 inclusions")
+AnnotationAssertion(rdfs:label obo:DOID_0060672 "GRN-related frontotemporal lobar degeneration with Tdp43 inclusions")
 SubClassOf(obo:DOID_0060672 obo:DOID_9255)
 SubClassOf(obo:DOID_0060672 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))