@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI> .
@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/v4.0.0/void/> .

dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_head {
  this: np:hasAssertion dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_assertion;
    np:hasProvenance dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_provenance;
    np:hasPublicationInfo dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_assertion a np:Assertion .
  
  dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_provenance a np:Provenance .
  
  dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_assertion {
  miriam-gene:3064 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGN06b35187112d65ad6695366c606b911f sio:SIO_000628 miriam-gene:3064, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_provenance {
  dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_assertion dcterms:description
      "[As a Mendelian neurodegenerative disorder, the genetic risk of Huntington's disease (HD) is conferred entirely by an HTT CAG repeat expansion whose length is the primary determinant of the rate of pathogenesis leading to disease onset.]. 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:26232222;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:31+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}