@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_head {
  this: np:hasAssertion dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_assertion;
    np:hasProvenance dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_provenance;
    np:hasPublicationInfo dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_assertion a np:Assertion .
  
  dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_provenance a np:Provenance .
  
  dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_assertion {
  miriam-gene:1861 a ncit:C16612 .
  
  lld:C0752203 a ncit:C7057 .
  
  dgn-gda:DGNcd29a7397e5158c92605602ea466b4a5 sio:SIO_000628 miriam-gene:1861, lld:C0752203;
    a sio:SIO_001121 .
}

dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_provenance {
  dgn-np:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_assertion dcterms:description
      "[Overall, our findings do not support the hypothesis that common TOR1A variants affect susceptibility for sporadic primary dystonia, and that it is unlikely that common variants around the DYT genes confer substantial risk for sporadic primary dystonia.]. 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:22172551;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP946960.RAF_kUzEu9CVkzd43LXGLCrHGFF3kGGkpjtCOnebvUFe8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:54+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}