@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I> .
@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:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_head {
  this: np:hasAssertion dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_assertion;
    np:hasProvenance dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_provenance;
    np:hasPublicationInfo dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_assertion a np:Assertion .
  
  dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_provenance a np:Provenance .
  
  dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_assertion {
  miriam-gene:1822 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGNe567d489acaa48390321b9a551db2ffd sio:SIO_000628 miriam-gene:1822, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_provenance {
  dgn-np:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_assertion dcterms:description
      "[The aim of this study was to perform DNA analysis in patients with clinical diagnosis of Huntington's disease (HD) after molecular exclusion of HD and further molecular examinations for other neurodegenerative diseases such as Huntington's disease-like 2 (HDL-2; gene JPH3), dentatorubral pallidoluysian atrophy (DRPLA; gene ATN1) and spinocerebellar ataxia type 17 (SCA17; gene TBP).]. 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:18651325;
    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:NP170205.RACgkyJTcztYTvOSOTU7qXeV9I1eIjcaT_uIx2fu_AP2I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+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" .
}