@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs> .
@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:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_head {
  this: np:hasAssertion dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_assertion;
    np:hasProvenance dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_provenance;
    np:hasPublicationInfo dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_assertion a np:Assertion .
  
  dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_provenance a np:Provenance .
  
  dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_assertion {
  miriam-gene:3065 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGNc75cfb159f6b20a07be6f103f24b0a52 sio:SIO_000628 miriam-gene:3065, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_provenance {
  dgn-np:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_assertion dcterms:description
      "[A transgenic primate model for Huntington's Disease (HD) first reported by our group that (HD monkeys) carry the mutant Huntingtin (HTT) gene with expanded polyglutamine (CAG) repeats and, develop chorea, dystonia, and other involuntary motor deficiencies similar to HD [ 1 ].]. 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:23190281;
    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:NP812953.RAT3nDvic6i3mhO2JBbDI0R9T7UsenQDjQnD22-R-uXBs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:18+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" .
}