@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y> .
@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:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_head {
  this: np:hasAssertion dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_assertion;
    np:hasProvenance dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_provenance;
    np:hasPublicationInfo dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_assertion a np:Assertion .
  
  dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_provenance a np:Provenance .
  
  dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_assertion {
  miriam-gene:54751 a ncit:C16612 .
  
  lld:C0031069 a ncit:C7057 .
  
  dgn-gda:DGNccf696b1d77b817c19fb3bf87c8f8e45 sio:SIO_000628 miriam-gene:54751, lld:C0031069;
    a sio:SIO_001121 .
}

dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_provenance {
  dgn-np:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_assertion dcterms:description
      "[We investigated a possible association between Kawasaki disease (KD), a systemic vasculitis of unknown etiology, or its coronary artery lesions (CAL) and MEFV gene variants including E148Q, the most common and mild mutation in the MEFV gene for familial Mediterranean fever or vasculitis-related disorders.]. 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:19026701;
    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:NP836477.RAje5HrLxlPwBvuXP8hde0mqd_dw-4Ssxx0dyaFPBxX0Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:31+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" .
}