@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY> .
@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#> .
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  this: np:hasAssertion dgn-np:NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY130_assertion ;
    np:hasProvenance dgn-np:NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY130_provenance ;
    np:hasPublicationInfo dgn-np:NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY130_provenance a np:Provenance .
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}
dgn-np:NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY130_assertion {
  miriam-gene:5243 a ncit:C16612 .
  lld:C0041696 a ncit:C7057 .
  dgn-gda:DGN546c974af9848a3cb90a6208f343e261 sio:SIO_000628 miriam-gene:5243 , lld:C0041696 ;
    a sio:SIO_001121 .
}
dgn-np:NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY130_provenance {
  dgn-np:NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY130_assertion dcterms:description "[In order to resolve these inconsistencies, we conducted a study in a large cohort of patients with major depressive disorder with the aim to unravel the association of ABCB1 variants with adverse effects of antidepressants and in particular with selective serotonin reuptake inhibitors (SSRIs), which display affinity as substrate for P-gp.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP165525.RAnKFnaB6OIlQKgJzqIsvWb0wUwkQzckkE_izTZi6g5WY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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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