@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs> .
@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:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_head {
  this: np:hasAssertion dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_assertion;
    np:hasProvenance dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_provenance;
    np:hasPublicationInfo dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_assertion a np:Assertion .
  
  dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_provenance a np:Provenance .
  
  dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0162534 a ncit:C7057 .
  
  dgn-gda:DGNf6513c559439eb0462d370791ce2bcd3 sio:SIO_000628 miriam-gene:5621, lld:C0162534;
    a sio:SIO_001122 .
}

dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_provenance {
  dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_assertion dcterms:description
      "[Indeed, the phenotypical expression of two of the most common mutations in the human PRNP gene associated with genetic prion diseases, D178N and E200K, is clearly modulated by the codon 129 polymorphism.]. 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:19684471;
    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:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:28+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" .
}