@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_head {
  this: np:hasAssertion dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_assertion;
    np:hasProvenance dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_provenance;
    np:hasPublicationInfo dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_assertion a np:Assertion .
  
  dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_provenance a np:Provenance .
  
  dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C0002726 a ncit:C7057 .
  
  dgn-gda:DGN329bda37d1e984a9c30350e6987a998a sio:SIO_000628 miriam-gene:3918, lld:C0002726;
    a sio:SIO_001121 .
}

dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_provenance {
  dgn-np:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_assertion dcterms:description
      "[After the exclusion of other hereditary fever syndromes, migraine, stroke, Molaret's meningitis, Behçet's syndrome and mitochondriopathy by clinical, serological, CSF investigations, funduscopy, electroencephalography, and cerebral MRI and MRI angiography, the described neurological abnormalities were regarded as CNS and PNS manifestation of vasculitis or amyloidosis in FMF.]. 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:12189462;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP530656.RAHN8YoKu-o5v_7Tvl-_aMvlD8dhy_ExgNscnjvOowPbU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:54+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}