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license |
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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.
mild ATP8B1 deficiency
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0009469 |
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BRIC1
|
0009469 |
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Summerskill syndrome
|
0009469 |
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Bric type 1
|
0009469 |
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benign recurrent intrahepatic cholestasis 1
|
0009469 |
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recurrent familial intrahepatic cholestasis 1
|
0009469 |
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benign recurrent intrahepatic cholestasis caused by mutation in ATP8B1
|
0009469 |
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benign recurrent intrahepatic cholestasis type 1
|
0009469 |
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cholestasis, benign recurrent intrahepatic 1
|
0009469 |
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ATP8B1 benign recurrent intrahepatic cholestasis
|
0009469 |
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cholestasis, benign recurrent intrahepatic, 1
|
0009469 |
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cholestasis, benign recurrent intrahepatic, type 1
|
0009469 |
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