@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_head
{
this:
np:hasAssertion
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_assertion
;
np:hasProvenance
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_provenance
;
np:hasPublicationInfo
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_assertion
a
np:Assertion
.
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_provenance
a
np:Provenance
.
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C1096063
a
ncit:C7057
.
dgn-gda:DGN63ad174c460a9f9bc43f0a99f5f670ac
sio:SIO_000628
miriam-gene:1557
,
lld:C1096063
;
a
sio:SIO_001121
.
}
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_provenance
{
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_assertion
dcterms:description
"[We aimed to evaluate the association of non-response to antiepileptic pharmacotherapy with the frequency of variant alleles in the drug transporter genes ABCB1 and ABCC2 or in the CYP2C locus in young patients with epilepsy and an independent cohort of adults with drug-refractory epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19415824
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP322232.RAe0u-7BYs5y8JO1cU1sSOpMF8iMlCsoSBuEwccCgnTBs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:08+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}