@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0> .
@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:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_head {
  this: np:hasAssertion dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_assertion ;
    np:hasProvenance dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_provenance ;
    np:hasPublicationInfo dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_assertion a np:Assertion .
  dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_provenance a np:Provenance .
  dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  lld:C0162534 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_provenance {
  dgn-np:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_assertion dcterms:description "[Recent studies have focused on the role of different isoforms of the disease-associated human prion protein and the effects of the naturally occurring polymorphism at codon 129 in the human prion protein gene on the conversion process, improving our understanding of the interaction between host and agent factors that influence the wide range of phenotypes in human prion diseases.]. 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:20535485 ;
    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:NP817648.RAECjbag9rJ4SRPYw08QYaXnWgvhLZ79-Hw_Js2bd0vS0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:55+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
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}