@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E> .
@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/v3.0.0/void/> .

dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_head {
  this: np:hasAssertion dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_assertion;
    np:hasProvenance dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_provenance;
    np:hasPublicationInfo dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_assertion a np:Assertion .
  
  dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_provenance a np:Provenance .
  
  dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_assertion {
  miriam-gene:55532 a ncit:C16612 .
  
  lld:C0752203 a ncit:C7057 .
  
  dgn-gda:DGN137e1bbb3a3406176f215554a2d1f087 sio:SIO_000628 miriam-gene:55532, lld:C0752203;
    a sio:SIO_001121 .
}

dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_provenance {
  dgn-np:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_assertion dcterms:description
      "[In just over a year, four new genes have been shown to cause primary dystonia (CIZ1, ANO3, TUBB4A and GNAL), PRRT2 has been identified as the cause of paroxysmal kinesigenic dystonia and other genes, such as SLC30A10 and ATP1A3, have been linked to more complicated forms of dystonia or new phenotypes.]. 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:23775978;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP919019.RAejsq_E-4n2eJSVEqoWU9lkNnEB_S3vCxQvMsahtkR-E130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:01+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}