@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM> .
@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:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_head {
  this: np:hasAssertion dgn-np:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_assertion ;
    np:hasProvenance dgn-np:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_provenance ;
    np:hasPublicationInfo dgn-np:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_provenance a np:Provenance .
  dgn-np:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_assertion {
  miriam-gene:5243 a ncit:C16612 .
  lld:C0014556 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_provenance {
  dgn-np:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_assertion dcterms:description "[Several explanations for refractory TLE are (1) an overexpression of P-glycoprotein (P-gp) encoded by multiple drug resistance 1 (MDR1) gene and other efflux transporters such as multidrug resistance protein (MRP) in the cerebrovascular endothelium in or around the region of the epileptic focus may lead to drug resistance in epilepsy; (2) the loss of antiepileptic drug sensitivity at certain target sites in the brain, including the sodium ion channel and the gamma aminobutyric acid (GABA)A receptor; and (3) seizures beget seizures by means of a cascade of events that include various types of neuronal damage, sprouting of neuronal axons and new synapse formations that establish aberrant glutamatergic synapses.]. 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:19960958 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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  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:NP647989.RA9hxs5DiYjqKn0KZOoHMN2s4MHQ3hHPpYPB9uFGkn1CM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:30+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> ;
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}