@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4> .
@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:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_head {
  this: np:hasAssertion dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_assertion;
    np:hasProvenance dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_provenance;
    np:hasPublicationInfo dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_assertion a np:Assertion .
  
  dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_provenance a np:Provenance .
  
  dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_assertion {
  miriam-gene:834 a ncit:C16612 .
  
  lld:C0268390 a ncit:C7057 .
  
  dgn-gda:DGN359ee52262a926aa9a14d18f6a01511b sio:SIO_000628 miriam-gene:834, lld:C0268390;
    a sio:SIO_001121 .
}

dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_provenance {
  dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_assertion dcterms:description
      "[The autoinflammatory disorders Muckle-Wells syndrome, familial cold urtecaria and chronic infantile neurological cutaneous and articular syndrome are associated with mutations in the NALP3 (Cryopyrin) gene, which is the central platform of the proinflammatory caspase-1 activating complex, named the inflammasome.]. 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:17431422;
    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:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:15+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" .
}