@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A> .
@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:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_head {
  this: np:hasAssertion dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_assertion;
    np:hasProvenance dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_provenance;
    np:hasPublicationInfo dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_assertion a np:Assertion .
  
  dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_provenance a np:Provenance .
  
  dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_assertion {
  miriam-gene:3064 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGNc438a1fdedbb08b6dc473d54f38289cc sio:SIO_000628 miriam-gene:3064, lld:C0020179;
    a sio:SIO_001122 .
}

dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_provenance {
  dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_assertion dcterms:description
      "[Use of RNA interference to reduce huntingtin protein (htt) expression in affected brain regions may provide an effective treatment for Huntington disease (HD), but it remains uncertain whether suppression of both wild-type and mutant alleles in a heterozygous patient will provide more benefit than harm.]. 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:19289118;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:19+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" .
}