@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk> .
@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:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_head {
  this: np:hasAssertion dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_assertion;
    np:hasProvenance dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_provenance;
    np:hasPublicationInfo dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_assertion a np:Assertion .
  
  dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_provenance a np:Provenance .
  
  dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C1852467 a ncit:C7057 .
  
  dgn-gda:DGN7e5eb293d305e75fcbc1c89c0594ec6f sio:SIO_000628 miriam-gene:5621, lld:C1852467;
    a sio:SIO_001121 .
}

dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_provenance {
  dgn-np:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_assertion dcterms:description
      "[Sporadic Creutzfeldt-Jakob disease (sCJD) is characterized by wide clinical and pathological variability, which is mainly influenced by the conformation of the misfolded prion protein (PrPSc) and by methionine and valine polymorphism at codon 129 of the gene encoding PrP.]. 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:23780662;
    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:NP1087221.RAi567PuQ8AOZ77fHWd22DIXYXm_Guq-sy6KTikYf8oxk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:59+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" .
}