Merge branch 'main' of https://github.com/DiseaseOntology/HumanDiseaseOntology

- integrating versions

Author: lschriml

src/ontology/doid-edit.owl

@@ -42694,9 +42694,7 @@ SubClassOf(obo:DOID_0061032 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0061033 (autosomal dominant intellectual developmental disorder 59)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/30184290/") obo:IAO_0000115 obo:DOID_0061033 "An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the CAMK2G gene on chromosome 10q22.
-
-")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/30184290/") obo:IAO_0000115 obo:DOID_0061033 "An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the CAMK2G gene on chromosome 10q22.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061033 "MIM:618522")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061033 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0061033 "DOID:0061033")
@@ -42746,9 +42744,7 @@ SubClassOf(obo:DOID_0061037 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0061038 (autosomal dominant intellectual developmental disorder 65)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/33232677/") obo:IAO_0000115 obo:DOID_0061038 "An autosomal dominant intellectual developmental disorder characterized by delayed motor and speech acquisition, variably impaired intellectual development, and behavioral abnormalities that has_material_basis_in heterozygous mutation in the KDM4B gene on chromosome 19p13.
-
-")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/33232677/") obo:IAO_0000115 obo:DOID_0061038 "An autosomal dominant intellectual developmental disorder characterized by delayed motor and speech acquisition, variably impaired intellectual development, and behavioral abnormalities that has_material_basis_in heterozygous mutation in the KDM4B gene on chromosome 19p13.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061038 "MIM:619320")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061038 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0061038 "DOID:0061038")
@@ -42768,9 +42764,7 @@ SubClassOf(obo:DOID_0061039 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0061040 (autosomal dominant intellectual developmental disorder 67)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/35675825/") obo:IAO_0000115 obo:DOID_0061040 "An autosomal dominant intellectual developmental disorder characterized by global developmental delay with variably impaired intellectual development apparent from infancy or early childhood that has_material_basis_in heterozygous mutation in the GRIA1 gene on chromosome 5q33.
-
-")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/35675825/") obo:IAO_0000115 obo:DOID_0061040 "An autosomal dominant intellectual developmental disorder characterized by global developmental delay with variably impaired intellectual development apparent from infancy or early childhood that has_material_basis_in heterozygous mutation in the GRIA1 gene on chromosome 5q33.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061040 "MIM:619927")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061040 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0061040 "DOID:0061040")