@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg> .
@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:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_head {
  this: np:hasAssertion dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_assertion;
    np:hasProvenance dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_provenance;
    np:hasPublicationInfo dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_assertion a np:Assertion .
  
  dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_provenance a np:Provenance .
  
  dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_assertion {
  miriam-gene:9730 a ncit:C16612 .
  
  lld:C0085281 a ncit:C7057 .
  
  dgn-gda:DGNcf4c17e4485cee4d80148fbc7e0442cf sio:SIO_000628 miriam-gene:9730, lld:C0085281;
    a sio:SIO_001121 .
}

dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_provenance {
  dgn-np:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_assertion dcterms:description
      "[The TaqIA single-nucleotide polymorphism (SNP), which is the most widely studied genetic polymorphism in addictions, is located at the gene that encodes the RIP kinase ANKK1 near the gene for dopamine receptor D2.]. 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:20845092;
    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:NP785676.RA8zfRzZ6pvnGNtKEmhmQfXmPHSi27P9E8aQPBMP41-kg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:56+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" .
}