@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY> .
@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:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_head {
  this: np:hasAssertion dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_assertion;
    np:hasProvenance dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_provenance;
    np:hasPublicationInfo dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_assertion a np:Assertion .
  
  dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_provenance a np:Provenance .
  
  dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGN7b3a00458a6c4cd95e24932d772a2af8 sio:SIO_000628 miriam-gene:5621, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_provenance {
  dgn-np:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_assertion dcterms:description
      "[This case implies a worldwide distribution of FFI and also highlights the need for more aggressive clinical application of genomic analysis of the PrP gene and polysomnographic study in patients with insomnia and cognitive impairments.]. 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:8909448;
    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:NP180847.RAyuEZyvWMcqcFtfDrQ91_RZAbF1iWl8mwHwYmQGSQaNY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}