@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY> .
@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:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_head {
  this: np:hasAssertion dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_assertion;
    np:hasProvenance dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_provenance;
    np:hasPublicationInfo dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_assertion a np:Assertion .
  
  dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_provenance a np:Provenance .
  
  dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_assertion {
  miriam-gene:1244 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN0cc68682a0bb5796ae3b2df6b1e1a86d sio:SIO_000628 miriam-gene:1244, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_provenance {
  dgn-np:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_assertion dcterms:description
      "[We have evaluated the functional polymorphisms of ABCB1, ABCG2, and ABCC2 genes with regard to epilepsy drug response in partial epilepsy, and have investigated the potential of combined effects of polymorphisms in more than one transporter gene.]. 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:19167193;
    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:NP273443.RATB_tP3VhReJGjwIFquKcwIhWfjI8bnSkEoP1GaMxLgY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:34+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" .
}