@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ> .
@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:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_head {
  this: np:hasAssertion dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_assertion;
    np:hasProvenance dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_provenance;
    np:hasPublicationInfo dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_assertion a np:Assertion .
  
  dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_provenance a np:Provenance .
  
  dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0162534 a ncit:C7057 .
  
  dgn-gda:DGN40951720da1a461b1b3279e07cf4aa53 sio:SIO_000628 miriam-gene:5621, lld:C0162534;
    a sio:SIO_001122 .
}

dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_provenance {
  dgn-np:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_assertion dcterms:description
      "[ The results of this study confirm that the different polymorphism at codon 129 of the PRNP gene, which could be involved in the structural domains of human PrP, might modulate the pathological phenotype of TSE.]. 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:11220690;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52695.RAPtyZgk50Ym8FLcn53cR_z-twK82u8-HPXy7GWwIDxqQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}