DOs August release

DiseaseOntology · Aug 21, 2020 · 519ae92 · 519ae92
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Showing 112 changed files with 2,907,440 additions and 12,938 deletions.
diff --git a/src/ontology/EQdiffAug.tsv b/src/ontology/EQdiffAug.tsv
diff --git a/src/ontology/HumanDO.obo b/src/ontology/HumanDO.obo
diff --git a/src/ontology/HumanDO.owl b/src/ontology/HumanDO.owl
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -49871,7 +49871,7 @@ SubClassOf(obo:DOID_0080706 obo:DOID_0050902)
 
 # Class: obo:DOID_0080707 (medulloblastoma non-WNT/non-SHH group 3)
 
-AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url: https://pubmed.ncbi.nlm.nih.gov/30876441/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/29427151/") obo:IAO_0000115 obo:DOID_0080707 "A medulloblastoma non-WNT/non-SHH that is characterized as a molecular subtype by absent TP53 mutations and MYC amplifications that may be present.")
+AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/29427151/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/30876441/") obo:IAO_0000115 obo:DOID_0080707 "A medulloblastoma non-WNT/non-SHH that is characterized as a molecular subtype by absent TP53 mutations and MYC amplifications that may be present.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080707 "NCI:C129445")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080707 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080707 "DOID:0080707")
@@ -49928,8 +49928,8 @@ SubClassOf(obo:DOID_0080712 obo:DOID_0050177)
 
 # Class: obo:DOID_0080713 (MECP2 duplication syndrome)
 
+AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://ghr.nlm.nih.gov/condition/mecp2-duplication-syndrome") Annotation(oboInOwl:hasDbXref "url:https://rarediseases.info.nih.gov/diseases/9781/mecp2-duplication-syndrome") obo:IAO_0000115 obo:DOID_0080713 "A syndrome that has_material_basis_in an extra copy of the MECP2 gene in each cell, occurs almost exclusively in males and that is characterized by delayed development of motor skills such as sitting and walking.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080713 "GARD:9781")
-AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://ghr.nlm.nih.gov/condition/mecp2-duplication-syndrome") Annotation(oboInOwl:hasDbXref "url:https://rarediseases.info.nih.gov/diseases/9781/mecp2-duplication-syndrome") oboInOwl:hasOBONamespace obo:DOID_0080713 "A syndrome that has_material_basis_in an extra copy of the MECP2 gene in each cell, occurs almost exclusively in males and that is characterized by delayed development of motor skills such as sitting and walking.")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080713 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080713 "DOID:0080713")
 AnnotationAssertion(rdfs:label obo:DOID_0080713 "MECP2 duplication syndrome"@en)

diff --git a/src/ontology/doid-merged.obo b/src/ontology/doid-merged.obo