@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg> .
@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:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_head {
  this: np:hasAssertion dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_assertion;
    np:hasProvenance dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_provenance;
    np:hasPublicationInfo dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_assertion a np:Assertion .
  
  dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_provenance a np:Provenance .
  
  dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_assertion {
  miriam-gene:2688 a ncit:C16612 .
  
  lld:C0022336 a ncit:C7057 .
  
  dgn-gda:DGNfc9b1ddf6b26fe2f7b8c9b21098726ae sio:SIO_000628 miriam-gene:2688, lld:C0022336;
    a sio:SIO_001121 .
}

dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_provenance {
  dgn-np:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_assertion dcterms:description
      "[We tested DNA from 15 centrally infected cases of iatrogenic Creutzfeldt-Jakob disease (CJD) (dura mater or corneal homografts and stereotactic EEG electrodes), 11 peripherally infected cases (native human growth hormone or gonadotrophin), and 110 control individuals for the presence of mutations in the chromosome 20 amyloid gene.]. 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:8309577;
    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:NP292400.RAcyYPC1BkFnYlpOfwZLsnF30JBfFP6YI-r0_YxbfvRjg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:46+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" .
}