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2 changes: 1 addition & 1 deletion docs/metrics/doid.md
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**IRI:** http://purl.obolibrary.org/obo/mondo/sources/doid.owl

**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-19/doid.owl
**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-26/doid.owl

### Entities and axioms

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2 changes: 1 addition & 1 deletion docs/metrics/gard.md
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**IRI:** http://purl.obolibrary.org/obo/mondo/sources/gard.owl

**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-19/gard.owl
**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-26/gard.owl

### Entities and axioms

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2 changes: 1 addition & 1 deletion docs/metrics/icd10cm.md
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**IRI:** http://purl.obolibrary.org/obo/mondo/sources/icd10cm.owl

**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-19/icd10cm.owl
**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-26/icd10cm.owl

### Entities and axioms

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2 changes: 1 addition & 1 deletion docs/metrics/icd10who.md
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**IRI:** http://purl.obolibrary.org/obo/mondo/sources/icd10who.owl

**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-19/icd10who.owl
**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-26/icd10who.owl

### Entities and axioms

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2 changes: 1 addition & 1 deletion docs/metrics/ncit.md
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**IRI:** http://purl.obolibrary.org/obo/mondo/sources/ncit.owl

**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-19/ncit.owl
**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-26/ncit.owl

### Entities and axioms

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20 changes: 10 additions & 10 deletions docs/metrics/omim.md
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**IRI:** http://purl.obolibrary.org/obo/mondo/sources/omim.owl

**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-20/omim.owl
**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-26/omim.owl

### Entities and axioms

| Metric | Value |
| ------ | ----- |
| Annotation properties | 13 |
| Axioms | 347642 |
| Logical axioms | 36016 |
| Classes | 31451 |
| Axioms | 347785 |
| Logical axioms | 36036 |
| Classes | 31466 |
| Object properties | 6 |
| Data properties | 0 |
| Individuals | 0 |
Expand All @@ -32,16 +32,16 @@

| Metric | Value |
| ------ | ----- |
| AnnotationAssertion | 280160 |
| Declaration | 31466 |
| SubClassOf | 36016 |
| AnnotationAssertion | 280268 |
| Declaration | 31481 |
| SubClassOf | 36036 |


#### Entity namespaces: axiom counts by namespace

| Metric | Value |
| ------ | ----- |
| prefix_unknown | 30006 |
| prefix_unknown | 30021 |
| oboInOwl | 3 |
| owl | 2 |
| xsd | 1 |
Expand All @@ -60,8 +60,8 @@

| Metric | Value |
| ------ | ----- |
| Class | 103477 |
| ObjectSomeValuesFrom | 14185 |
| Class | 103532 |
| ObjectSomeValuesFrom | 14192 |


More information about the source can be found [in the documentation](../sources.md). The raw data (ontology metrics) can be found [on GitHub](https://github.com/monarch-initiative/mondo-ingest/tree/main/src/ontology/metadata).
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2 changes: 1 addition & 1 deletion docs/metrics/ordo.md
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**IRI:** http://purl.obolibrary.org/obo/mondo/sources/ordo.owl

**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-20/ordo.owl
**Version IRI:** http://purl.obolibrary.org/obo/mondo/sources/2023-08-26/ordo.owl

### Entities and axioms

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6 changes: 3 additions & 3 deletions docs/reports/migrate.md
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# Migratable terms
| Ontology | Tot |
|:----------------------------------|:------|
| [DOID](./migrate_doid.md) | 95 |
| [DOID](./migrate_doid.md) | 96 |
| [GARD](./migrate_gard.md) | 9,370 |
| [ORDO](./migrate_ordo.md) | 3 |
| [NCIT](./migrate_ncit.md) | 2,113 |
| [ICD10WHO](./migrate_icd10who.md) | 119 |
| [ORDO](./migrate_ordo.md) | 110 |
| [OMIM](./migrate_omim.md) | 101 |
| [OMIM](./migrate_omim.md) | 110 |
| [ICD10CM](./migrate_icd10cm.md) | 1,889 |

### Codebook
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11 changes: 6 additions & 5 deletions docs/reports/migrate_doid.md
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| MONDO:0956997 | oligodendroglioma, idh-mutant and 1p/19q-codeleted, grade 3 | DOID:0081282 | MONDO:equivalentTo | oligodendroglioma, IDH-mutant and 1p/19q-codeleted, grade 3 | An IDH-mutant, and 1p/19q-codeleted oligodendroglioma that is characterized as grade 3 tumors associated with a more rapid growth. Grade 3 tumors appear to have abnormalities on chromosomes 9 or 10, along with unusual amounts of growth factors and proteins, which are thought to contribute to the more rapid growth of these gliomas. | MONDO:0859592 |
| MONDO:0957118 | bradyopsia 2 | DOID:0070364 | MONDO:equivalentTo | bradyopsia 2 | | MONDO:0012033 |
| MONDO:0957120 | nevoid basal cell carcinoma syndrome 2 | DOID:0070366 | MONDO:equivalentTo | nevoid basal cell carcinoma syndrome 2 | | MONDO:0007187 |
| MONDO:0957121 | leukoencephalopathy with vanishing white matter 5 | DOID:0070367 | MONDO:equivalentTo | leukoencephalopathy with vanishing white matter 5 | | MONDO:0011380 |
| MONDO:0957122 | leukoencephalopathy with vanishing white matter 4 | DOID:0070371 | MONDO:equivalentTo | leukoencephalopathy with vanishing white matter 4 | | MONDO:0011380 |
| MONDO:0957123 | leukoencephalopathy with vanishing white matter 3 | DOID:0070372 | MONDO:equivalentTo | leukoencephalopathy with vanishing white matter 3 | | MONDO:0011380 |
| MONDO:0957124 | leukoencephalopathy with vanishing white matter 2 | DOID:0070373 | MONDO:equivalentTo | leukoencephalopathy with vanishing white matter 2 | | MONDO:0011380 |
| MONDO:0957121 | leukoencephalopathy with vanishing white matter 5 | DOID:0070367 | MONDO:equivalentTo | leukoencephalopathy with vanishing white matter 5 | | MONDO:0800448 |
| MONDO:0957122 | leukoencephalopathy with vanishing white matter 4 | DOID:0070371 | MONDO:equivalentTo | leukoencephalopathy with vanishing white matter 4 | | MONDO:0800448 |
| MONDO:0957123 | leukoencephalopathy with vanishing white matter 3 | DOID:0070372 | MONDO:equivalentTo | leukoencephalopathy with vanishing white matter 3 | | MONDO:0800448 |
| MONDO:0957124 | leukoencephalopathy with vanishing white matter 2 | DOID:0070373 | MONDO:equivalentTo | leukoencephalopathy with vanishing white matter 2 | | MONDO:0800448 |
| MONDO:0957127 | developmental and epileptic encephalopathy 31b | DOID:0070376 | MONDO:equivalentTo | developmental and epileptic encephalopathy 31B | | MONDO:0100062|MONDO:0006025 |
| MONDO:0957181 | epidermolytic hyperkeratosis 2 | DOID:0081359 | MONDO:equivalentTo | epidermolytic hyperkeratosis 2 | An epidermolytic hyperkeratosis that is characterized by generalized erythema, erosions, scaling, and easily breaking blisters that become less frequent later in life, while hyperkeratosis increases and that has_material_basis_in heterozygous or homozygous mutation in the keratin-10 gene (KRT10) on chromosome 17q21. | MONDO:0007239 |
| MONDO:0957195 | digenic disease | DOID:0080578 | MONDO:equivalentTo | digenic disease | | |
Expand Down Expand Up @@ -99,4 +99,5 @@
| MONDO:0957522 | nemaline myopathy 5c | DOID:0081375 | MONDO:equivalentTo | nemaline myopathy 5C | A nemaline myopathy that has_material_basis_in autosomal dominant inheritance of a homozygous or compound heterozygous mutation in the TNNT1 gene on chromosome 19q13. | MONDO:0018958|MONDO:0000426 |
| MONDO:0957523 | sorbitol dehydrogenase deficiency with peripheral neuropathy | DOID:0081376 | MONDO:equivalentTo | sorbitol dehydrogenase deficiency with peripheral neuropathy | A neuromuscular disease that is characterized by onset of distal muscle weakness mainly affecting the lower limbs and resulting in difficulty walking and that has_material_basis_in homozygous or compound heterozygous mutation in the SORD gene on chromosome 15q21. | MONDO:0019056|MONDO:0006025 |
| MONDO:0957524 | cox deficiency, benign infantile mitochondrial myopathy | DOID:0081377 | MONDO:equivalentTo | COX deficiency, benign infantile mitochondrial myopathy | A cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles. | MONDO:0009068 |
| MONDO:0957525 | kyphosis | DOID:4667 | MONDO:equivalentTo | kyphosis | | MONDO:0000836|MONDO:0000812 |
| MONDO:0957525 | kyphosis | DOID:4667 | MONDO:equivalentTo | kyphosis | | MONDO:0000836|MONDO:0000812 |
| MONDO:0957558 | li-fraumeni syndrome 1 | DOID:0111503 | MONDO:equivalentTo | Li-Fraumeni syndrome 1 | | MONDO:0018875 |
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