@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U> .
@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:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_head {
  this: np:hasAssertion dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_assertion;
    np:hasProvenance dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_provenance;
    np:hasPublicationInfo dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_assertion a np:Assertion .
  
  dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_provenance a np:Provenance .
  
  dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0085220 a ncit:C7057 .
  
  dgn-gda:DGN0883ff2ed3d2221db30c00109e581b4a sio:SIO_000628 miriam-gene:5621, lld:C0085220;
    a sio:SIO_001121 .
}

dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_provenance {
  dgn-np:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_assertion dcterms:description
      "[Stop codon mutations in the gene encoding the prion protein (PRNP) are very rare and have thus far only been described in two patients with prion protein cerebral amyloid angiopathy (PrP-CAA).]. 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:19911184;
    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:NP193262.RAPrCGfT5iwkBSwMrtzcRPwBamn5KGOyttiPQ0JP1Zx5U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:46+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" .
}