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Namespace Prefixes

PrefixIRI
n9http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0029998/
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n2http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/
dctermshttp://purl.org/dc/terms/
n10http://www.emea.europa.eu/docs/cs_CZ/document_library/EPAR_-_Product_Information/human/000797/
n3http://linked.opendata.cz/ontology/sukl/
skoshttp://www.w3.org/2004/02/skos/core#
n4http://linked.opendata.cz/resource/sukl/indgroup/
n5http://linked.opendata.cz/resource/sukl/packing/
n8http://linked.opendata.cz/resource/sukl/company/
n7http://linked.opendata.cz/resource/sukl/active-ingredient/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n6http://linked.opendata.cz/resource/sukl/registration-state/
xsdhhttp://www.w3.org/2001/XMLSchema#
n15http://linked.opendata.cz/resource/sukl/df/
n12http://linked.opendata.cz/resource/atc/

Statements

Subject Item
n2:0029998
rdf:type
n3:MedicinalProductPackaging
dcterms:title
ATRIPLA 600 MG/200 MG/245 MG
skos:notation
0029998
n3:hasATCCode
n12:J05AR06
n3:hasActiveIngredient
n7:EFAVIRENZUM n7:TENOFOVIRI-DISOPROXILI-FUMARAS n7:EMTRICITABINUM
n3:hasDefinedDailyDose
n9:ddd
n3:hasDosageForm
n15:TBL-FLM-POR
n3:hasPackagingSize
30
n3:hasPacking
n5:TBC
n3:hasRegistrationHolder
n8:BXBIRL
n3:hasRegistrationState
n6:R
n3:hasRouteOfAdministration
n14:POR
n3:hasStrength
n3:hasIndicationGroup
n4:42
n3:containsDefinedDailyDoses
30.0
n3:hasRegistrationCode
EU/1/07/430/001
n3:hasTitleSupplement
POR TBL FLM 30
n3:pilFile
http%3A%2F%2Fwww.emea.europa.eu%2Fdocs%2Fcs_CZ%2Fdocument_library%2FEPAR_-_Product_Information%2Fhuman%2F000797%2FWC500028102.pdf
n3:pilUri
n10:WC500028102.pdf
n3:spcFile
http%3A%2F%2Fwww.emea.europa.eu%2Fdocs%2Fcs_CZ%2Fdocument_library%2FEPAR_-_Product_Information%2Fhuman%2F000797%2FWC500028102.pdf
n3:spcUri
n10:WC500028102.pdf