@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs> .
@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:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_head {
  this: np:hasAssertion dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_assertion;
    np:hasProvenance dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_provenance;
    np:hasPublicationInfo dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_assertion a np:Assertion .
  
  dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_provenance a np:Provenance .
  
  dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_assertion {
  miriam-gene:1861 a ncit:C16612 .
  
  lld:C0242422 a ncit:C7057 .
  
  dgn-gda:DGN1ea7285dc91135021ca443b5f5385e12 sio:SIO_000628 miriam-gene:1861, lld:C0242422;
    a sio:SIO_001121 .
}

dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_provenance {
  dgn-np:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_assertion dcterms:description
      "[Our data suggest that the DYT1 mutation is not associated with significant damage to the nigrostriatal DA system, in keeping with the absence of parkinsonism and levodopa response in this disorder.]. 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:10720299;
    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:NP456118.RAK0atIi6M4F12gSgEfd56sRvPHhGbUghAZsyF5HyHyjs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:32+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" .
}