@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI> .
@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:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_head {
  this: np:hasAssertion dgn-np:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_assertion;
    np:hasProvenance dgn-np:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_provenance;
    np:hasPublicationInfo dgn-np:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_provenance a np:Provenance .
  
  dgn-np:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_assertion {
  miriam-gene:23627 a ncit:C16612 .
  
  lld:C0022336 a ncit:C7057 .
  
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dgn-np:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_provenance {
  dgn-np:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_assertion dcterms:description
      "[Our study evaluated previous findings of the association of SNPs in the PRNP and PRND genes in the largest cohorts for association study in sCJD to date, and extends previous findings by defining for the first time the haplotypes associated with sCJD in a large population of the German CJD surveillance study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP407696.RAjRNWQL1Ul1UP1nvGYYxI0LH0HJF0CLKX_3M__krWfpI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:02+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>,
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}