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identifiers-org-data-collection.json
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identifiers-org-data-collection.json
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{
"@context": {
"dcat": "http://www.w3.org/ns/dcat#",
"idot": "http://identifiers.org/terms#",
"foaf": "http://xmlns.com/foaf/0.1/",
"schema": "http://schema.org/",
"vcard": "http://www.w3.org/2001/vcard-rdf/3.0#",
"dcterms": "http://purl.org/dc/terms/"
},
"@type": "DataCollection",
"schema:creator": {
"@type": "schema:Person",
"schema:email": "[email protected]"
},
"schema:editor": {
"@type": "schema:Person",
"schema:email": "[email protected]"
},
"dcat:issued": "2016-03-11T17:39:47+00:00",
"dcat:modified": "2016-03-11T17:53:35+00:00",
"idot:lastChecked": "2016-03-15T14:45:34+00:00",
"schema:url": "http://www.ebi.ac.uk/miriam/main/collections/MIR:00000571",
"dcat:title": "Human Phenotype Ontology",
"dcterms:alternative": "HPO",
"dcat:identifier": "MIR:00000571",
"idot:identifierScheme": {
"idot:namespace": "hpo",
"dcterms:alternative": "HPO",
"schema:uri": "http://identifiers.org/hpo/",
"idot:example": "HP:0000118",
"idot:identifierPatterns": "^HP:\\d{7}$",
"idot:alternativeIdentifierSchemes": ["urn:miriam:hpo", "http://purl.obolibrary.org/obo/HP"]
},
"idot:primaryLocation": {
"dcat:description": "Human Phenotype Ontology at Institute for Medical Genetics and Human Genetics",
"schema:url": "http://compbio.charite.de/hpoweb/showterm?id=$id",
"vcard:orgName": "Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin, Berlin, Germany",
"schema:url": "http://human-phenotype-ontology.github.io/",
"idot:reliability": "0"
},
"idot:alternativeLocations": [
{
"dcat:description":"Human Phenotype Ontology through OLS",
"schema:url": "http://www.ebi.ac.uk/ols/beta/ontologies/hp/terms?obo_id=$id",
"vcard:orgName": "European Bioinformatics Institute, Hinxton, Cambridge, UK",
"schema:url": "http://www.ebi.ac.uk/ols/beta/ontologies/hp",
"idot:reliability": "100"
}
],
"schema:url": "http://www.ebi.ac.uk/ols/beta/ontologies/hp",
"dcat:description": "The Human Phenotype Ontology (HPO) aims to provide a standardized vocabulary of phenotypic abnormalities encountered in human disease. Each term in the HPO describes a phenotypic abnormality, such as atrial septal defect. The HPO is currently being developed using the medical literature, Orphanet, DECIPHER, and OMIM."
}