@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko> .
@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:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_head {
  this: np:hasAssertion dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_assertion;
    np:hasProvenance dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_provenance;
    np:hasPublicationInfo dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_assertion a np:Assertion .
  
  dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_provenance a np:Provenance .
  
  dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_assertion {
  miriam-gene:4210 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN9f778c6368abe20bdc83684ab5db4bee sio:SIO_000628 miriam-gene:4210, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_provenance {
  dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_assertion dcterms:description
      "[MEFV mutation carriage appears to modify the SLE disease phenotype in that it contributes to an excess of inflammatory manifestations such as fever and pleuritis on the one hand, while thwarting more severe renal involvement on the other.]. 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:22532615;
    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:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:27+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" .
}