@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0> .
@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:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_head {
  this: np:hasAssertion dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_assertion;
    np:hasProvenance dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_provenance;
    np:hasPublicationInfo dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_assertion a np:Assertion .
  
  dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_provenance a np:Provenance .
  
  dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0027765 a ncit:C7057 .
  
  dgn-gda:DGN5ad19bbbb5b704d64d4b49c71cf24a3d sio:SIO_000628 miriam-gene:4397, lld:C0027765;
    a sio:SIO_001121 .
}

dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_provenance {
  dgn-np:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_assertion dcterms:description
      "[There is not currently evidence for shared causation or pathogenesis between the two neurological disorders but we will follow with interest the emerging genetic characterization of parkin in both PD and MS.]. 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:22523156;
    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:NP526929.RAOIoGfv2vTnWd0qLjr76RHP7IjdAN17sbmBJgKvhM4P0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:16+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" .
}