@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY> .
@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:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_head {
  this: np:hasAssertion dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_assertion;
    np:hasProvenance dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_provenance;
    np:hasPublicationInfo dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_assertion a np:Assertion .
  
  dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_provenance a np:Provenance .
  
  dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGNfc878c0afc16a698bbc2b58cf47b3b29 sio:SIO_000628 miriam-gene:5621, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_provenance {
  dgn-np:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_assertion dcterms:description
      "[Fatal familial insomnia (FFI) is an inherited prion disease characterized by progressive insomnia and dysautonomia with only modest cognitive impairment early in the disease, associated with atrophy and gliosis in the medial thalamus, but without spongiform change.]. 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:9270595;
    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:NP694115.RAb6jfhg_-bQOzdn3JhKAwXDBf4GXcwIWUFWPbpdqewSY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:02+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" .
}