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

 #
   -- aligning versions of edit file

Author: lschriml

src/ontology/doid-edit.owl

@@ -32435,7 +32435,7 @@ SubClassOf(obo:DOID_0060270 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0060271 (pontocerebellar hypoplasia type 2E)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007636) Annotation(oboInOwl:hasDbXref "url:https://www.omim.org/entry/615851") obo:IAO_0000115 obo:DOID_0060271 "A pontocerebellar hypoplasia that is characterized by progressive microcephaly, profound intellectual disability, spasticity and seizure, has_material_basis_in autosomal recessive inheritance of mutation in the VPS53 gene.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007636) Annotation(oboInOwl:hasDbXref "url:https://www.omim.org/entry/615851") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/24577744/") obo:IAO_0000115 obo:DOID_0060271 "A pontocerebellar hypoplasia that is characterized by profoundly impaired intellectual development, progressive microcephaly, spasticity, and early-onset epilepsy that has_material_basis_incompound heterozygous mutation in the VPS53 gene on chromosome 17p13.")
 AnnotationAssertion(oboInOwl:created_by obo:DOID_0060271 "emitraka")
 AnnotationAssertion(oboInOwl:creation_date obo:DOID_0060271 "2015-02-04T14:28:28Z")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060271 "MIM:615851")
@@ -80104,7 +80104,7 @@ SubClassOf(obo:DOID_0110715 ObjectSomeValuesFrom(obo:RO_0004019 obo:HP_0001197))
 
 # Class: obo:DOID_0110716 (Warburg micro syndrome 1)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/20512159") obo:IAO_0000115 obo:DOID_0110716 "A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/20512159") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/20512159/") obo:IAO_0000115 obo:DOID_0110716 "A Warburg micro syndrome characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, optic atrophy, cortical dysplasia, in particular corpus callosum hypoplasia, severely impaired intellectual development, spastic diplegia, and hypogonadism that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110716 "ICD10CM:Q87.0")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0110716 "MIM:600118")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0110716 "Micro Syndrome 1")