@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U> .
@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:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_head {
  this: np:hasAssertion dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_assertion;
    np:hasProvenance dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_provenance;
    np:hasPublicationInfo dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_assertion a np:Assertion .
  
  dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_provenance a np:Provenance .
  
  dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_assertion {
  miriam-gene:4261 a ncit:C16612 .
  
  lld:C1290884 a ncit:C7057 .
  
  dgn-gda:DGNfe3721bea660983be0ce9cd2ea4d7b1b sio:SIO_000628 miriam-gene:4261, lld:C1290884;
    a sio:SIO_001121 .
}

dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_provenance {
  dgn-np:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_assertion dcterms:description
      "[Notably, genetic variation in the genes encoding the NOD proteins NOD2, cryopyrin and CIITA (MHC class II transactivator) in humans and Naip5 (neuronal apoptosis inhibitory protein 5) in mice is associated with inflammatory disease or increased susceptibility to bacterial infections.]. 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:12766759;
    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:NP707712.RAoPAd_BY8cINIkh36tO-69dCLMhO6PTpATMwgQzos__U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:10+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" .
}