@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY> .
@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:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_head {
  this: np:hasAssertion dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_assertion;
    np:hasProvenance dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_provenance;
    np:hasPublicationInfo dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_assertion a np:Assertion .
  
  dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_provenance a np:Provenance .
  
  dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_assertion {
  miriam-gene:6513 a ncit:C16612 .
  
  lld:C1970149 a ncit:C7057 .
  
  dgn-gda:DGN48c55a84d8645475ca81701579fc731f sio:SIO_000628 miriam-gene:6513, lld:C1970149;
    a sio:SIO_001121 .
}

dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_provenance {
  dgn-np:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_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:NP847257.RAGvJd4zwPJQASqo6EC5g2Ps1VSjlDBZIRX0qLAJgWBgY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:38+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" .
}