@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE> .
@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:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_head {
  this: np:hasAssertion dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_assertion;
    np:hasProvenance dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_provenance;
    np:hasPublicationInfo dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_assertion a np:Assertion .
  
  dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_provenance a np:Provenance .
  
  dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0022336 a ncit:C7057 .
  
  dgn-gda:DGNe17c5cfed796e9c45fd3848f98650631 sio:SIO_000628 miriam-gene:5621, lld:C0022336;
    a sio:SIO_001122 .
}

dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_provenance {
  dgn-np:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_assertion dcterms:description
      "[The purpose of this study was (1) to detect asymptomatic carriers of the prion protein gene mutation E200K, which is associated with Creutzfeldt-Jakob disease (CJD), in corneal donors and in the general population of Slovakia and (2) to assess the genetic testing of corneal donors as an effective preventive measure against iatrogenic infection in a country with an unusually high incidence of genetic CJD.]. 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:21508834;
    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:NP888727.RA5zj4CbM06xcYLRhVJWqQ8WR1TsKivHiX06hVKyPzrPE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:27+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" .
}