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Namespace Prefixes

PrefixIRI
n8http://linked.opendata.cz/resource/sukl/roa/
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dctermshttp://purl.org/dc/terms/
n5http://www.ema.europa.eu/docs/cs_CZ/document_library/EPAR_-_Product_Information/human/002549/
n3http://linked.opendata.cz/ontology/sukl/
skoshttp://www.w3.org/2004/02/skos/core#
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n9http://linked.opendata.cz/resource/sukl/packing/
n15http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0193883/
n6http://linked.opendata.cz/resource/sukl/company/
n4http://linked.opendata.cz/resource/sukl/active-ingredient/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
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xsdhhttp://www.w3.org/2001/XMLSchema#
n14http://linked.opendata.cz/resource/sukl/df/
n7http://linked.opendata.cz/resource/atc/

Statements

Subject Item
n2:0193883
rdf:type
n3:MedicinalProductPackaging
dcterms:title
TOLUCOMBI 80 MG/12,5 MG
skos:notation
0193883
n3:hasATCCode
n7:C09DA07
n3:hasActiveIngredient
n4:TELMISARTANUM n4:HYDROCHLOROTHIAZIDUM
n3:hasDefinedDailyDose
n15:ddd
n3:hasDosageForm
n14:TBL-NOB-POR
n3:hasPackagingSize
14 II
n3:hasPacking
n9:BLI
n3:hasRegistrationHolder
n6:KRKSLO
n3:hasRegistrationState
n13:R
n3:hasRouteOfAdministration
n8:POR
n3:hasStrength
80MG/12.5MG
n3:hasIndicationGroup
n10:58
n3:containsDefinedDailyDoses
14.0
n3:hasRegistrationCode
EU/1/13/821/013
n3:hasTitleSupplement
POR TBL NOB 14
n3:spcFile
http%3A%2F%2Fwww.ema.europa.eu%2Fdocs%2Fcs_CZ%2Fdocument_library%2FEPAR_-_Product_Information%2Fhuman%2F002549%2FWC500141639.pdf
n3:spcUri
n5:WC500141639.pdf