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created at |
2021-12-20 14:06:07 UTC |
updated at |
2021-12-22 07:06:57 UTC |
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PREFIX owl: <http://www.w3.org/2002/07/owl#>
PREFIX rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#>
PREFIX rdfs: <http://www.w3.org/2000/01/rdf-schema#>
PREFIX obo: <http://www.geneontology.org/formats/oboInOwl#>
SELECT DISTINCT ?label (SUBSTR(str(?sub),38) AS ?id) WHERE {
?sub rdfs:subClassOf+ <http://purl.obolibrary.org/obo/MONDO_0000001> ;
rdf:type owl:Class .
{ { ?sub rdfs:label ?label }
UNION { ?sub obo:hasBroadSynonym ?label }
UNION { ?sub obo:hasExactSynonym ?label }
UNION { ?sub obo:hasRelatedSynonym ?label }
}
}
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110,360 entries
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There is 0 pattern entry.
AMC
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0015168 |
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myodysplasia
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0015168 |
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Arthromyodysplasia congenita
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0015168 |
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Guerin-Stern syndrome
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0015168 |
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Guérin-Stern syndrome
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0015168 |
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Otto syndrome
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0015168 |
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Rossi syndrome
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0015168 |
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amyoplasia congenita
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0015168 |
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congenital amyoplasia
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0015168 |
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congenital arthromyodysplasia
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0015168 |
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rocher-Sheldon syndrome
|
0015168 |
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multiple congenital arthrogryposis
|
0015168 |
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arthrogryposis multiplex congenita
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0015168 |
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myodystrophia fetalis deformans
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0015168 |
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fibrous ankylosis of multiple joints
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0015168 |
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