identifiers-org-with-edam.json

{
  "@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/",
    "edam": "http://edamontology.org/"
  },
  "@type": "DataCollection",
  "schema:creator": 
  {
    "@type": "schema:Person",
    "schema:email": "someone@somewhere.com"
  },
  "schema:editor": 
  {
    "@type": "schema:Person",
    "schema:email": "person@anywhere.com"
  },
  "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/ols/beta/ontologies/hp",
  "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"
    ],
  "edam": "data_1087",
  "edam": "format_2331", 
  },
  "idot:primaryLocation": 
  {
    "dcat:description": "Human Phenotype Ontology at Institute for Medical Genetics and Human Genetics",
    "schema:url": "http://human-phenotype-ontology.github.io/",
    "vcard:orgName": "Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin, Berlin, Germany",
    "idot:reliability": "0"
  },
  "idot:alternativeLocations": 
  [
    {
      "dcat:description": "Human Phenotype Ontology through OLS",
      "schema:url": "http://www.ebi.ac.uk/ols/beta/ontologies/hp",
      "vcard:orgName": "European Bioinformatics Institute, Hinxton, Cambridge, UK",
      "idot:reliability": "100"
    }
  ],

  "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.",
  "edam": "topic_0089",
  "edam": "topic_2815",
  "edam": "topic_0634"
}