@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4> .
@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:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_head {
  this: np:hasAssertion dgn-np:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_assertion ;
    np:hasProvenance dgn-np:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_provenance ;
    np:hasPublicationInfo dgn-np:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_provenance a np:Provenance .
  dgn-np:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_assertion {
  miriam-gene:23627 a ncit:C16612 .
  lld:C1852467 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_provenance {
  dgn-np:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_assertion dcterms:description "[To answer the question of whether there are any polymorphisms within the PrP-like protein gene (Prnd) that might cause or be involved in the development of TSEs, we investigated the complete open reading frame of the human Prnd gene from 58 patients who had died of genetic or sporadic Creutzfeldt-Jakob disease (CJD), Alzheimer's disease or other neurological disorders and from 111 controls.]. 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:11702213 ;
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  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:NP876567.RA5B8dgBC1r9CBKybBoDmtW7Bgl-D68cgZF-fALneYgx4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:33+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}