|
gptkbp:instanceOf
|
gptkb:online_learning_platform
gptkb:database
|
|
gptkbp:abbreviation
|
gptkb:Orphanet
|
|
gptkbp:focusesOn
|
orphan drugs
rare diseases
|
|
gptkbp:foundedBy
|
gptkb:Ségolène_Aymé
|
|
gptkbp:foundedIn
|
1997
|
|
gptkbp:headquartersLocation
|
gptkb:Paris,_France
|
|
gptkbp:language
|
gptkb:Bulgarian
gptkb:Estonian
gptkb:French
gptkb:German
gptkb:Greek
gptkb:Italian
gptkb:Norwegian
gptkb:Romanian
gptkb:Spanish
gptkb:Latvian
gptkb:Slovenian
Croatian
Czech
Dutch
English
Finnish
Hungarian
Icelandic
Lithuanian
Polish
Portuguese
Swedish
Turkish
Slovak
|
|
gptkbp:license
|
CC BY 4.0
|
|
gptkbp:operatedBy
|
gptkb:INSERM
|
|
gptkbp:partOf
|
gptkb:European_Reference_Networks
|
|
gptkbp:provides
|
gptkb:insurance
clinical trials information
epidemiological data
expert centers directory
genetic testing information
orphan drug information
patient organizations directory
|
|
gptkbp:recognizedBy
|
gptkb:ORPHA
|
|
gptkbp:supportedBy
|
gptkb:European_Parliament
|
|
gptkbp:supportsFormat
|
gptkb:RDF
gptkb:JSON
XML
CSV
|
|
gptkbp:targetUser
|
gptkb:researchers
policy makers
patients
pharmaceutical industry
clinicians
|
|
gptkbp:website
|
https://www.orpha.net/
|
|
gptkbp:bfsParent
|
gptkb:Online_Mendelian_Inheritance_in_Man_(OMIM)
gptkb:Cowden_syndrome
|
|
gptkbp:bfsLayer
|
6
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
Orphanet
|