@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU> .
@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:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_head {
  this: np:hasAssertion dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_assertion;
    np:hasProvenance dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_provenance;
    np:hasPublicationInfo dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_assertion a np:Assertion .
  
  dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_provenance a np:Provenance .
  
  dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_assertion {
  miriam-gene:50818 a ncit:C16612 .
  
  lld:C1970238 a ncit:C7057 .
  
  dgn-gda:DGN24b60a03a5740288749fddb9d5cc0bd4 sio:SIO_000628 miriam-gene:50818, lld:C1970238;
    a sio:SIO_001121 .
}

dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_provenance {
  dgn-np:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_assertion dcterms:description
      "[Three additional autosomal dominant forms (DYT9, DYT19 and DYT20) might exist based on linkage mapping to regions apparently different from, yet in close proximity to or overlapping with the known loci DYT18, DYT10 and DYT8.]. 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:19578124;
    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:NP892714.RAZ9yrAghNPk8Pw84echeHWnAs55NkYpdmb1kpcTGT_CU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:08+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" .
}