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gptkbp:instanceOf
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gptkb:database
online learning platform
|
|
gptkbp:abbreviation
|
gptkb:Orphanet
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|
gptkbp:focusesOn
|
orphan drugs
rare diseases
|
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gptkbp:foundedBy
|
gptkb:Ségolène_Aymé
|
|
gptkbp:foundedIn
|
1997
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gptkbp:headquartersLocation
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gptkb:Paris,_France
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https://www.w3.org/2000/01/rdf-schema#label
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Orphanet
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gptkbp:language
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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
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gptkbp:operatedBy
|
gptkb:INSERM
|
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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
|
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gptkbp:recognizedBy
|
gptkb:ORPHA
|
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gptkbp:supportedBy
|
gptkb:European_Parliament
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gptkbp:supportsFormat
|
gptkb:RDF
gptkb:JSON
XML
CSV
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gptkbp:targetUser
|
gptkb:researchers
policy makers
patients
pharmaceutical industry
clinicians
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gptkbp:website
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https://www.orpha.net/
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gptkbp:bfsParent
|
gptkb:NCBI_Gene
gptkb:Online_Mendelian_Inheritance_in_Man_(OMIM)
gptkb:Cowden_syndrome
|
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gptkbp:bfsLayer
|
6
|