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Namespace Prefixes

PrefixIRI
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dctermshttp://purl.org/dc/terms/
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n12http://www.emea.europa.eu/docs/cs_CZ/document_library/EPAR_-_Product_Information/human/000725/
n16http://linked.opendata.cz/resource/sukl/specialization-restriction/
skoshttp://www.w3.org/2004/02/skos/core#
n11http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0029232/price-of-originator/
n21http://linked.opendata.cz/resource/sukl/indgroup/
n6http://linked.opendata.cz/resource/sukl/packing/
n15http://linked.opendata.cz/resource/sukl/company/
n5http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0029232/reimbursement/
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n9http://linked.opendata.cz/resource/sukl/specialization-restriction/http://linked.opendata.cz/ontology/odcs/tabular/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
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n13http://linked.opendata.cz/resource/sukl/registration-state/
n7http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0029232/price/
xsdhhttp://www.w3.org/2001/XMLSchema#
n20http://linked.opendata.cz/resource/atc/
n14http://linked.opendata.cz/resource/sukl/df/

Statements

Subject Item
n2:0029232
rdf:type
n3:MedicinalProductPackaging
dcterms:title
BINOCRIT 5000 IU/0,5 ML
skos:notation
0029232
n3:hasATCCode
n20:B03XA01
n3:hasActiveIngredient
n10:EPOETINUM-ALFA
n3:hasDefinedDailyDose
n17:ddd
n3:hasDosageForm
n14:INJ-SOL-ISP-SDR-IVN
n3:hasPackagingSize
1X0.5ML I
n3:hasPacking
n6:ISP
n3:hasRegistrationHolder
n15:SZKA
n3:hasRegistrationState
n13:R
n3:hasRouteOfAdministration
n19:SDR-IVN
n3:hasStrength
10000IU/ML
n3:hasIndicationGroup
n21:12
n3:hasSpecializationRestriction
n9:blank-cell n16:NEF n16:INT n16:HEM n16:PED n16:ONK
n3:containsDefinedDailyDoses
5.0
n3:hasRegistrationCode
EU/1/07/410/009
n3:hasTitleSupplement
SDR+IVN INJ SOL ISP 1X0.5ML I
n3:containsUsualTherapeuticalDailyDoses
5
n3:hasCoreReimbursementSpecification
n4:2013-01-01 n4:2013-01-05 n4:2013-04-01 n4:2013-05-01 n4:2013-02-01 n4:2013-03-01 n4:2013-08-01 n4:2013-08-03 n4:2013-06-01 n4:2013-07-01 n4:2013-11-01 n4:2013-12-01 n4:2013-09-01 n4:2013-10-01 n4:2014-03-01 n4:2014-04-01 n4:2014-01-01 n4:2014-02-01 n4:2014-05-01
n3:hasIndicationRestriction
P
n3:hasPriceOfOriginatorSpecification
n11:2014-04-01 n11:2014-05-01 n11:2014-02-01 n11:2014-03-01 n11:2013-12-01 n11:2014-01-01 n11:2013-10-01 n11:2013-11-01 n11:2013-08-03 n11:2013-09-01 n11:2013-07-01 n11:2013-08-01 n11:2013-05-01 n11:2013-06-01 n11:2013-03-01 n11:2013-04-01 n11:2013-01-05 n11:2013-02-01 n11:2013-01-01
n3:hasPriceSpecification
n7:2013-11-01 n7:2013-12-01 n7:2014-01-01 n7:2014-02-01 n7:2014-03-01 n7:2014-04-01 n7:2014-05-01 n7:2013-04-01 n7:2013-05-01 n7:2013-06-01 n7:2013-07-01 n7:2013-08-01 n7:2013-08-03 n7:2013-09-01 n7:2013-10-01 n7:2013-01-01 n7:2013-01-05 n7:2013-02-01 n7:2013-03-01
n3:hasReimbursementSpecification
n5:2013-03-01 n5:2013-04-01 n5:2013-01-05 n5:2013-02-01 n5:2013-07-01 n5:2013-08-01 n5:2013-05-01 n5:2013-06-01 n5:2013-01-01 n5:2014-04-01 n5:2014-05-01 n5:2013-10-01 n5:2013-11-01 n5:2013-08-03 n5:2013-09-01 n5:2014-02-01 n5:2014-03-01 n5:2013-12-01 n5:2014-01-01
n3:hasUsualTherapeuticalDailyDose
n17:utdd
n3:spcFile
http%3A%2F%2Fwww.emea.europa.eu%2Fdocs%2Fcs_CZ%2Fdocument_library%2FEPAR_-_Product_Information%2Fhuman%2F000725%2FWC500053680.pdf
n3:spcUri
n12:WC500053680.pdf