@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs> .
@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:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_head {
  this: np:hasAssertion dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_assertion;
    np:hasProvenance dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_provenance;
    np:hasPublicationInfo dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_assertion a np:Assertion .
  
  dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_provenance a np:Provenance .
  
  dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C2936349 a ncit:C7057 .
  
  dgn-gda:DGN1939b06abeb0826adb98817dfd23daac sio:SIO_000628 miriam-gene:5621, lld:C2936349;
    a sio:SIO_001121 .
}

dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_provenance {
  dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_assertion dcterms:description
      "[Six cases had a mutation at codon 102 of the prion protein (PrP) gene and in these the characteristic pathology was the formation of multicentric amyloid plaques which were stained with PrP antibody, whereas spongiform changes were absent in one and minimal in two.]. 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:8355811;
    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:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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" .
}