@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE> .
@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:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_head {
  this: np:hasAssertion dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_assertion ;
    np:hasProvenance dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_provenance ;
    np:hasPublicationInfo dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_provenance a np:Provenance .
  dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  lld:C0022336 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_provenance {
  dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_assertion dcterms:description "[The relationships between the degree of cortical prion protein (PrP) deposition, tissue vacuolation and astrocytosis were studied in the frontal cortex of 27 cases of human spongiform encephalopathy, encompassing 13 cases of sporadic Creutzfeldt-Jakob disease (sCJD), four cases of familial CJD (fCJD) (one owing to E200K mutation, one owing to 144 bp insertion, one owing to P102L mutation and one owing to A117V mutation), five cases of iatrogenic CJD (iCJD) owing to growth hormone therapy and five cases of variant CJD (vCJD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP586234.RA7Rd6ras3-kY3GYyE3UPpdou9-DSusOCC5Q9AzG24juE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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> ;
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}