@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA> .
@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:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_head {
  this: np:hasAssertion dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_assertion;
    np:hasProvenance dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_provenance;
    np:hasPublicationInfo dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_assertion a np:Assertion .
  
  dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_provenance a np:Provenance .
  
  dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_assertion {
  miriam-gene:23400 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN7e6caacfdbb501122daa851f6680b9d9 sio:SIO_000628 miriam-gene:23400, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_provenance {
  dgn-np:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_assertion dcterms:description
      "[Using voxel-based morphometry in 30 asymptomatic mutation carriers (MC) with mutations in four different genes for PD and 100 healthy controls, we identified an increase in gray matter volume (GMV) in the striatum in asymptomatic Parkin, PINK1, ATP13A2 and, to a much lesser extent, in LRRK2 MC.]. 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:20483373;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP67025.RARyCyXn3P8jKOLXucS_GNi6nFIyngLO9GECzNqVhVeoA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}