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Correct typo in trimethylaminuria definition for accuracy.
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csbjohnson committed Jan 6, 2025
1 parent 12aa422 commit 8e67d93
Showing 1 changed file with 1 addition and 1 deletion.
2 changes: 1 addition & 1 deletion src/ontology/doid-edit.owl
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Expand Up @@ -55067,7 +55067,7 @@ SubClassOf(obo:DOID_0080360 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014

# Class: obo:DOID_0080361 (trimethylaminuria)

AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(oboInOwl:hasDbXref "url:https://ghr.nlm.nih.gov/condition/trimethylaminuria") Annotation(oboInOwl:hasDbXref "url:https://www.genome.gov/Genetic-Disorders/Trimethylaminuria") obo:IAO_0000115 obo:DOID_0080361 "An inherited metabolic disorder characterized by the inabilty to break down trimethylamine and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding flavin-containing monooxygenase-3 on chromosome 1q24."@en)
AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(oboInOwl:hasDbXref "url:https://ghr.nlm.nih.gov/condition/trimethylaminuria") Annotation(oboInOwl:hasDbXref "url:https://www.genome.gov/Genetic-Disorders/Trimethylaminuria") obo:IAO_0000115 obo:DOID_0080361 "An inherited metabolic disorder characterized by the inability to break down trimethylamine and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding flavin-containing monooxygenase-3 on chromosome 1q24."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080361 "GARD:6447")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080361 "MESH:C536561")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080361 "MIM:602079")
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