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

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -28827,7 +28827,7 @@ SubClassOf(obo:DOID_0051053 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://medlineplus.gov/ency/article/000191.htm") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/38416090/") Annotation(oboInOwl:hasDbXref "url:https://www.annalsthoracicsurgery.org/article/S0003-4975(24)00077-8/fulltext") Annotation(oboInOwl:hasDbXref "url:https://www.mayoclinic.org/diseases-conditions/coarctation-of-the-aorta/symptoms-causes/syc-20352529") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/books/NBK430913/") Annotation(oboInOwl:hasDbXref "url:https://www.nyp.org/pediatrics/heart/coarctation-of-aorta") obo:IAO_0000115 obo:DOID_0051054 "A congenital heart disease that is characterized by the luminal narrowing of the thoracic aortic arch, typically located just beyond the left subclavian artery. This narrowing creates an obstruction that can lead to significant cardiovascular complications, including systemic hypertension, left ventricular hypertrophy, and eventually heart failure.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0051054 "MESH:D001017")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0051054 "MIM:120000")
-AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0051054 "NCIT:C84567")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0051054 "NCI:C84567")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0051054 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0051054 "DOID:0051054")
 AnnotationAssertion(rdfs:label obo:DOID_0051054 "coarctation of the aorta")
@@ -53196,12 +53196,14 @@ SubClassOf(obo:DOID_0070641 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/24388663/") obo:IAO_0000115 obo:DOID_0070642 "A hereditary spastic paraplegia that has_material_basis_in compound heterozygous mutation in the REEP2 gene on chromosome 5q31.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070642 "MIM:620606")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070642 "ORDO:401849")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0070642 "autosomal recessive spastic paraplegia 72")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0070642 "spastic paraplegia 72B")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0070642 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0070642 "DOID:0070642")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0070642 doid:DO_rare_slim)
 AnnotationAssertion(rdfs:label obo:DOID_0070642 "hereditary spastic paraplegia 72B")
+AnnotationAssertion(skos:broadMatch obo:DOID_0070642 "ORDO:401849")
 AnnotationAssertion(skos:exactMatch obo:DOID_0070642 "MIM:620606")
 SubClassOf(obo:DOID_0070642 obo:DOID_2476)
 SubClassOf(obo:DOID_0070642 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
@@ -82895,9 +82897,10 @@ AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0110817 "disease_ontology"
 AnnotationAssertion(oboInOwl:id obo:DOID_0110817 "DOID:0110817")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0110817 doid:DO_rare_slim)
 AnnotationAssertion(rdfs:label obo:DOID_0110817 "hereditary spastic paraplegia 72A")
+AnnotationAssertion(skos:broadMatch obo:DOID_0110817 "ICD10CM:G11.4")
+AnnotationAssertion(skos:broadMatch obo:DOID_0110817 "ORDO:401849")
 SubClassOf(obo:DOID_0110817 obo:DOID_2476)
 SubClassOf(obo:DOID_0110817 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
-SubClassOf(obo:DOID_0110817 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
 
 # Class: obo:DOID_0110818 (hereditary spastic paraplegia 73)