removed SNOMED IDs

DiseaseOntology · Aug 26, 2022 · ff8d5ff · ff8d5ff
1 parent 269c993
commit ff8d5ff
Showing 1 changed file with 1 addition and 5 deletions.
diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
@@ -41306,7 +41306,6 @@ AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasD
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070167 "MESH:D000072660"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070167 "NCI:C158500"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070167 "OMIM:102530"^^xsd:string)
-AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070167 "SNOMEDCT_US_2020_03_01:236818008"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0070167 "SPGF6"@en)
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0070167 "disease_ontology"^^xsd:string)
 AnnotationAssertion(oboInOwl:id obo:DOID_0070167 "DOID:0070167"^^xsd:string)
@@ -80016,7 +80015,6 @@ SubClassOf(obo:DOID_0111571 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/19365138"^^xsd:string) obo:IAO_0000115 obo:DOID_0111572 "A hair disease characterized by fine and tightly curled hair that grows slowly and stops growing after a few inches with hair shafts that display trichorrhexis nodosa and tapered ends."^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111572 "GARD:5597"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111572 "ORDO:170"^^xsd:string)
-AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111572 "SNOMEDCT_US_2020_03_01:52564001"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111572 "familial wooly hair syndrome"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111572 "hereditary woolly hair syndrome"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111572 "hereditary wooly hair syndrome"@en)
@@ -80031,6 +80029,7 @@ SubClassOf(obo:DOID_0111572 obo:DOID_421)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/20346438"^^xsd:string) obo:IAO_0000115 obo:DOID_0111573 "A familial woolly hair syndrome that has_material_basis_in heterozygous mutation in KRT74 on chromosome 12q13.13."^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111573 "OMIM:194300"^^xsd:string)
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111573 "SNOMEDCT_US_2022_07_31:403794008")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111573 "ADWH"@en)
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0111573 "disease_ontology"^^xsd:string)
 AnnotationAssertion(oboInOwl:id obo:DOID_0111573 "DOID:0111573"^^xsd:string)
@@ -80517,7 +80516,6 @@ AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111603 "MESH:C535857"^^xsd:stri
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111603 "OMIM:121070"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111603 "OMIM:158300"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111603 "ORDO:3377"^^xsd:string)
-AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111603 "SNOMEDCT_US_2020_03_01:8757006"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111603 "DA7"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111603 "Dutch-Kentucky syndrome"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111603 "Hecht syndrome"@en)
@@ -85343,7 +85341,6 @@ AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111947 "MESH:D000077428"^^xsd:s
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111947 "NCI:C126349"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111947 "OMIM:614172"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111947 "ORDO:228423"^^xsd:string)
-AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0111947 "SNOMEDCT_US_2020_03_01:778024005"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111947 "DCML"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111947 "GATA2 deficiency"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0111947 "IMD21"^^xsd:string)
@@ -115739,7 +115736,6 @@ AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_1339 "MESH:D029503"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_1339 "NCI:C61236"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_1339 "OMIM:PS105650"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_1339 "ORDO:124"^^xsd:string)
-AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_1339 "SNOMEDCT_US_2020_03_01:188588001"^^xsd:string)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_1339 "Blackfan - Diamond syndrome"@en)
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_1339 "chronic constitutional pure red cell anaemia"@en)
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_1339 "disease_ontology"^^xsd:string)