@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM> .
@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/v3.0.0/void/> .

dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_head {
  this: np:hasAssertion dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_assertion;
    np:hasProvenance dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_provenance;
    np:hasPublicationInfo dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_assertion a np:Assertion .
  
  dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_provenance a np:Provenance .
  
  dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0043528 a ncit:C7057 .
  
  dgn-gda:DGN41b631305ce3f549ff38b12811b75346 sio:SIO_000628 miriam-gene:5621, lld:C0043528;
    a sio:SIO_001121 .
}

dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_provenance {
  dgn-np:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_assertion dcterms:description
      "[The cause of sporadic Creutzfeldt-Jakob disease (CJD) is unknown, hereditary cases are associated with mutations of the prion protein gene (PRNP) and acquired forms are caused by the transmission of infection from human to human or, as a zoonosis, from cattle to human.]. 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:14522863;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP647514.RAYaP8uL21IN44YqVMc8vXWp-RZiQg8P7y3UfRrY4xcuM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:08+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}