@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc> .
@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:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_head {
  this: np:hasAssertion dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_assertion;
    np:hasProvenance dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_provenance;
    np:hasPublicationInfo dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_assertion a np:Assertion .
  
  dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_provenance a np:Provenance .
  
  dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_assertion {
  miriam-gene:1814 a ncit:C16612 .
  
  lld:C0270736 a ncit:C7057 .
  
  dgn-gda:DGNce535f83ad60960e08877f5a74507c76 sio:SIO_000628 miriam-gene:1814, lld:C0270736;
    a sio:SIO_001121 .
}

dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_provenance {
  dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_assertion dcterms:description
      "[These results suggest that DRD3 genotype and the variant DRD3Gly allelic variant is associated with the risk for and age at onset of ET, and with the risk for voice tremor, in Caucasian Spanish people.]. 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:19645064;
    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:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:38+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" .
}