@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM> .
@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:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_head {
  this: np:hasAssertion dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_assertion;
    np:hasProvenance dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_provenance;
    np:hasPublicationInfo dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_assertion a np:Assertion .
  
  dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_provenance a np:Provenance .
  
  dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_assertion {
  miriam-gene:139596 a ncit:C16612 .
  
  lld:C0270952 a ncit:C7057 .
  
  dgn-gda:DGN05065182a137bf15338a870afb4b8a65 sio:SIO_000628 miriam-gene:139596, lld:C0270952;
    a sio:SIO_001121 .
}

dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_provenance {
  dgn-np:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_assertion dcterms:description
      "[Further analysis of the cellular and molecular mechanisms by which UPP and molecular chaperones influence the degradation of misfolded proteins could provide novel concepts and targets for the treatment and understanding of the pathogenesis of OPMD and neurodegenerative diseases.]. 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:12944420;
    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:NP611334.RAeIK5mhFtjAmT3gyNgMo_H12NFcin-Z1H667MgPyPXbM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:09+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" .
}