@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU> .
@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:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_head {
  this: np:hasAssertion dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_assertion;
    np:hasProvenance dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_provenance;
    np:hasPublicationInfo dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_assertion a np:Assertion .
  
  dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_provenance a np:Provenance .
  
  dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  
  lld:C0040332 a ncit:C7057 .
  
  dgn-gda:DGN82a98b29b168a718b1d65ed767680cd3 sio:SIO_000628 miriam-gene:1813, lld:C0040332;
    a sio:SIO_001121 .
}

dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_provenance {
  dgn-np:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_assertion dcterms:description
      "[Studies examining the role of genetic variability in modulating individual response to nicotine in humans have increased, with recent work showing that genetic variation at the dopamine D2 receptor (DRD2) predicts response to pharmacotherapy for tobacco dependence.]. 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:16896957;
    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:NP848525.RAn25wDVyYheWOJheqDjnFSve9y-9qFk7VS4gpSWPxLJU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:38+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" .
}