@prefix bfo: <http://purl.obolibrary.org/obo/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg> .
@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 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:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_head {
  this: np:hasAssertion dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_assertion;
    np:hasProvenance dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_provenance;
    np:hasPublicationInfo dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_assertion a np:Assertion .
  
  dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_provenance a np:Provenance .
  
  dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0752353 a ncit:C7057 .
  
  dgn-gda:DGN197249e0bf972f71b0be174233734dde sio:SIO_000628 miriam-gene:367, lld:C0752353;
    a sio:SIO_001121 .
}

dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_provenance {
  dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_assertion dcterms:description
      "[Spinobulbar muscular atrophy and Huntington's disease are caused by polyglutamine expansion in the androgen receptor and huntingtin, respectively, and their pathogenesis has been associated with abnormal nuclear localization and aggregation of truncated forms of these proteins.]. 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:10639135;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy bfo:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a bfo:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP272720.RAjj-papy3UHSgQMqiuiwZlDedTnzUovXbn_MjW1ZZsLg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:49+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" .
}