@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I> .
@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:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_head {
  this: np:hasAssertion dgn-np:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_assertion ;
    np:hasProvenance dgn-np:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_provenance ;
    np:hasPublicationInfo dgn-np:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_assertion {
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dgn-np:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_provenance {
  dgn-np:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_assertion dcterms:description "[We describe the neuropsychological profiles of 10 cases and compare these data with cross sectional data obtained from patients with histologically confirmed sporadic CJD and cases with inherited prion disease with confirmed mutations in the prion protein gene.]. 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 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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dgn-np:NP212404.RA40A7xUWY80b9v8iHDjphmMX3jJbu-jmwn22HX6xcI-I130_publicationInfo {
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    dcterms:rightsHolder dgn-void:IBIGroup ;
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