@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA> .
@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:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_head {
  this: np:hasAssertion dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_assertion;
    np:hasProvenance dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_provenance;
    np:hasPublicationInfo dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_assertion a np:Assertion .
  
  dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_provenance a np:Provenance .
  
  dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_assertion {
  miriam-gene:1822 a ncit:C16612 .
  
  lld:C0087012 a ncit:C7057 .
  
  dgn-gda:DGNad63a252e72852bb7f331b6e1f2de944 sio:SIO_000628 miriam-gene:1822, lld:C0087012;
    a sio:SIO_001121 .
}

dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_provenance {
  dgn-np:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_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-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:NP361078.RAz-DLQJVRA3_YaSVeXA03pVmkwUFd_EMzSwIT4d2zxeA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:08+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: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" .
}