@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g> .
@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:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_head {
  this: np:hasAssertion dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_assertion;
    np:hasProvenance dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_provenance;
    np:hasPublicationInfo dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_assertion a np:Assertion .
  
  dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_provenance a np:Provenance .
  
  dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_assertion {
  miriam-gene:3064 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGNdd82ce27d7f34d36e48ab44c181f5856 sio:SIO_000628 miriam-gene:3064, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_provenance {
  dgn-np:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_assertion dcterms:description
      "[Huntington's disease (HD) is a neurodegenerative genetic disorder caused by an expansion of CAG repeats in the HD gene encoding for huntingtin (Htt), resulting in progressive death of striatal neurons, with clinical symptoms of chorea, dementia and dramatic weight loss.]. 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:22150069;
    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:NP788414.RAzBVY-s-RVNp-BmoU4T8YkWhG86Dfh0C7lTKlfpOX75g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:01+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" .
}