@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k> .
@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:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_head {
  this: np:hasAssertion dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion;
    np:hasProvenance dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance;
    np:hasPublicationInfo dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion a np:Assertion .
  
  dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance a np:Provenance .
  
  dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion {
  miriam-gene:23627 a ncit:C16612 .
  
  lld:C2931859 a ncit:C7057 .
  
  dgn-gda:DGN0b8df29bada3516237aeb88a911a742f sio:SIO_000628 miriam-gene:23627, lld:C2931859;
    a sio:SIO_001121 .
}

dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance {
  dgn-np:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion dcterms:description
      "[To investigate whether the PRND polymorphisms are associated with an increased risk for developing sporadic CJD in the Korean population, we compared the genotype and allele frequencies of PRND polymorphisms in 110 sporadic CJD patients with those in 102 healthy Koreans.]. 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:15933804;
    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:NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}