@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk> .
@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:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_head {
  this: np:hasAssertion dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_assertion;
    np:hasProvenance dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_provenance;
    np:hasPublicationInfo dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_assertion a np:Assertion .
  
  dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_provenance a np:Provenance .
  
  dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_assertion {
  miriam-gene:5132 a ncit:C16612 .
  
  lld:C0026650 a ncit:C7057 .
  
  dgn-gda:DGNc1c12ad47522ef0d2729461131fa9bc1 sio:SIO_000628 miriam-gene:5132, lld:C0026650;
    a sio:SIO_001121 .
}

dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_provenance {
  dgn-np:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_assertion dcterms:description
      "[Identifying the PDC locus on chromosome 2q will facilitate discovery of the PDC gene and enable investigators to determine whether PDC is genetically homogeneous and whether other paroxysmal movement disorders are also genetically linked to the PDC locus.]. 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:8659518;
    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:NP860467.RA9rXnK4GsYF3JOUPYFoA7hPEAppsul6E4as5YqpVTMqk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:46+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" .
}