minor classification updates

DiseaseOntology · Nov 6, 2023 · 3a1ab3f · 3a1ab3f
1 parent a3c1829
commit 3a1ab3f
Showing 1 changed file with 12 additions and 2 deletions.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -26745,7 +26745,7 @@ SubClassOf(obo:DOID_0050924 obo:DOID_4045)
 
 # Class: obo:DOID_0050925 (small intestine carcinoid neuroendocrine tumor)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007638) Annotation(oboInOwl:hasDbXref "url:http://en.wikipedia.org/wiki/Carcinoid") obo:IAO_0000115 obo:DOID_0050925 "A small intestine cancer that has_material_basis_in cells of the neuroendocrine system.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007638) Annotation(oboInOwl:hasDbXref "url:http://en.wikipedia.org/wiki/Carcinoid") obo:IAO_0000115 obo:DOID_0050925 "A neuroendocrine tumor that has_material_basis_in cells of the neuroendocrine system and that is located in the small intestine.")
 AnnotationAssertion(oboInOwl:created_by obo:DOID_0050925 "lschriml")
 AnnotationAssertion(oboInOwl:creation_date obo:DOID_0050925 "2014-10-21T12:58:08Z")
 AnnotationAssertion(oboInOwl:hasBroadSynonym obo:DOID_0050925 "intestinal carcinoid tumour")
@@ -26754,7 +26754,8 @@ AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0050925 "disease_ontology"
 AnnotationAssertion(oboInOwl:id obo:DOID_0050925 "DOID:0050925")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0050925 doid:DO_cancer_slim)
 AnnotationAssertion(rdfs:label obo:DOID_0050925 "small intestine carcinoid neuroendocrine tumor")
-SubClassOf(obo:DOID_0050925 obo:DOID_10154)
+SubClassOf(obo:DOID_0050925 obo:DOID_169)
+SubClassOf(obo:DOID_0050925 ObjectSomeValuesFrom(obo:RO_0004026 obo:UBERON_0002108))
 
 # Class: obo:DOID_0050926 (jejunal adenocarcinoma)
 
@@ -78456,6 +78457,7 @@ SubClassOf(obo:DOID_0111072 obo:DOID_66)
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/897853") obo:IAO_0000115 obo:DOID_0111073 "A heart conduction disease characterized by autosomal dominant inheritance of a cardiac conduction defect that may progress to complete atrioventricular (AV) block and maybe asymptomatic of manifest as shortness of breath, dizziness, syncope, abdominal pain, heart failure or sudden death.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111073 "OMIM:PS113900")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111073 "ORDO:871")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111073 "OMIM:115080")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111073 "PFHB"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111073 "familial Lenegre disease"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111073 "familial Lev disease"@en)
@@ -82331,6 +82333,9 @@ AnnotationAssertion(oboInOwl:id obo:DOID_0111350 "DOID:0111350")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0111350 doid:DO_rare_slim)
 AnnotationAssertion(rdfs:label obo:DOID_0111350 "Laurin-Sandrow syndrome")
 SubClassOf(obo:DOID_0111350 obo:DOID_1934)
+SubClassOf(obo:DOID_0111350 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
+SubClassOf(obo:DOID_0111350 ObjectSomeValuesFrom(obo:RO_0004026 obo:UBERON_0002387))
+SubClassOf(obo:DOID_0111350 ObjectSomeValuesFrom(obo:RO_0004026 obo:UBERON_0002398))
 
 # Class: obo:DOID_0111351 (D-2-hydroxyglutaric aciduria 1)
 
@@ -140096,12 +140101,17 @@ AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2436 "MESH:D005918")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2436 "NCI:C4222")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2436 "SNOMEDCT_US_2023_03_01:7429002")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2436 "UMLS_CUI:C0334421")
+AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/21163162/") oboInOwl:hasDbXref obo:DOID_2436 "A benign perivascular tumor that is a morphologic variant of the glomus tumor characterized by the presence of dilated veins, surrounded by small clusters of glomus cells. Glomangiomas are most often present in patients with multiple lesions.")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2436 "OMIM:138000")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2436 "ORDO:83454")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_2436 "Glomuvenous Malformation")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_2436 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_2436 "DOID:2436")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_2436 doid:DO_cancer_slim)
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_2436 doid:NCIthesaurus)
 AnnotationAssertion(rdfs:label obo:DOID_2436 "glomangioma")
 SubClassOf(obo:DOID_2436 obo:DOID_5238)
+SubClassOf(obo:DOID_2436 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
 
 # Class: obo:DOID_2437 (obsolete skin compound nevus)