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Remove unexpected newlines from definitions
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@allenbaron
allenbaron committed Jan 9, 2025
1 parent 8f68ac6 commit 8315f3b
Showing 1 changed file with 6 additions and 12 deletions.
18 changes: 6 additions & 12 deletions src/ontology/doid-edit.owl
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Expand Up @@ -54378,8 +54378,7 @@ SubClassOf(obo:DOID_0080296 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014

# Class: obo:DOID_0080297 (Coffin-Siris syndrome 6)

AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/28124119/") obo:IAO_0000115 obo:DOID_0080297 "A Coffin-Siris syndrome that is characterized by short stature, sparse hair, mild to severe intellectual disability, coarse facial features, and variable behavioral anomalies and that
has_material_basis_in heterozygous mutation in the ARID2 gene on chromosome 12q12."@en)
AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/28124119/") obo:IAO_0000115 obo:DOID_0080297 "A Coffin-Siris syndrome that is characterized by short stature, sparse hair, mild to severe intellectual disability, coarse facial features, and variable behavioral anomalies and that has_material_basis_in heterozygous mutation in the ARID2 gene on chromosome 12q12."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080297 "MIM:617808")
AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080297 "disease_ontology")
AnnotationAssertion(oboInOwl:id obo:DOID_0080297 "DOID:0080297")
Expand Down Expand Up @@ -58522,8 +58521,7 @@ SubClassOf(obo:DOID_0080654 obo:DOID_0080653)

# Class: obo:DOID_0080655 (hypophosphatemic nephrolithiasis/osteoporosis)

AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://www.nejm.org/doi/full/10.1056/NEJMoa020028") obo:IAO_0000115 obo:DOID_0080655 "A kidney disease that is characterized by formation of renal calcium
stones or bone demineralization."@en)
AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://www.nejm.org/doi/full/10.1056/NEJMoa020028") obo:IAO_0000115 obo:DOID_0080655 "A kidney disease that is characterized by formation of renal calcium stones or bone demineralization."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080655 "KEGG:H00888")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080655 "MIM:PS612286")
AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080655 "disease_ontology")
Expand Down Expand Up @@ -58905,8 +58903,7 @@ SubClassOf(obo:DOID_0080694 obo:DOID_225)

# Class: obo:DOID_0080695 (Burn-McKeown syndrome)

AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://ghr.nlm.nih.gov/condition/burn-mckeown-syndrome") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/books/NBK373577/") obo:IAO_0000115 obo:DOID_0080695 "A syndrome that is characterized by bilateral choanal atresia, cranio-facial dysmorphism,
hearing loss, heart abnormalities, and short stature."@en)
AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://ghr.nlm.nih.gov/condition/burn-mckeown-syndrome") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/books/NBK373577/") obo:IAO_0000115 obo:DOID_0080695 "A syndrome that is characterized by bilateral choanal atresia, cranio-facial dysmorphism, hearing loss, heart abnormalities, and short stature."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080695 "GARD:10041")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080695 "MESH:C537411")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080695 "MIM:608572")
Expand Down Expand Up @@ -59379,8 +59376,7 @@ SubClassOf(obo:DOID_0080733 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014

# Class: obo:DOID_0080734 (Ehlers-Danlos syndrome kyphoscoliotic type 1)

AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/28306229/") obo:IAO_0000115 obo:DOID_0080734 "An Ehlers-Danlos syndrome that is characterized by severe muscle hypotonia at birth, generalized joint laxity, scoliosis at birth, and scleral fragility and rupture of the ocular globe
and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding lysyl hydroxylase (PLOD1) on chromosome 1p36."@en)
AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/28306229/") obo:IAO_0000115 obo:DOID_0080734 "An Ehlers-Danlos syndrome that is characterized by severe muscle hypotonia at birth, generalized joint laxity, scoliosis at birth, and scleral fragility and rupture of the ocular globe and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding lysyl hydroxylase (PLOD1) on chromosome 1p36."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080734 "MIM:225400")
AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080734 "disease_ontology")
AnnotationAssertion(oboInOwl:id obo:DOID_0080734 "DOID:0080734")
Expand Down Expand Up @@ -60467,8 +60463,7 @@ SubClassOf(obo:DOID_0080836 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014

# Class: obo:DOID_0080837 (growth hormone insensitivity syndrome with immune dysregulation 2)

AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/29844444/") obo:IAO_0000115 obo:DOID_0080837 "A syndrome that is characterized by short stature due to insensitivity to growth hormone and
that has_material_basis_in heterozygous mutation in the STAT5B gene on chromosome 17q21."@en)
AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/29844444/") obo:IAO_0000115 obo:DOID_0080837 "A syndrome that is characterized by short stature due to insensitivity to growth hormone and that has_material_basis_in heterozygous mutation in the STAT5B gene on chromosome 17q21."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080837 "MIM:618985")
AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080837 "disease_ontology")
AnnotationAssertion(oboInOwl:id obo:DOID_0080837 "DOID:0080837")
Expand Down Expand Up @@ -184055,8 +184050,7 @@ SubClassOf(obo:DOID_6425 ObjectSomeValuesFrom(obo:RO_0004026 obo:UBERON_0001711)

# Class: obo:DOID_6428 (cervical adenoid basal carcinoma)

AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/10872669") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/25207054") obo:IAO_0000115 obo:DOID_6428 "A cervix carcinoma that has_material_basis_in epithelium and is characterized by the presence of small,
well differentiated, rounded nests of basaloid cells."@en)
AnnotationAssertion(Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/10872669") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/25207054") obo:IAO_0000115 obo:DOID_6428 "A cervix carcinoma that has_material_basis_in epithelium and is characterized by the presence of small, well differentiated, rounded nests of basaloid cells."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_6428 "NCI:C40213")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_6428 "SNOMEDCT_US_2023_03_01:763063001")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_6428 "UMLS_CUI:C1516403")
Expand Down

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