@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s> .
@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 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:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_head {
  this: np:hasAssertion dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_assertion;
    np:hasProvenance dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_provenance;
    np:hasPublicationInfo dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_assertion a np:Assertion .
  
  dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_provenance a np:Provenance .
  
  dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_assertion {
  miriam-gene:4792 a ncit:C16612 .
  
  lld:C0003872 a ncit:C7057 .
  
  dgn-gda:DGN3c160367c41ed3a124c57e63e5409311 sio:SIO_000628 miriam-gene:4792, lld:C0003872;
    a sio:SIO_001121 .
}

dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_provenance {
  dgn-np:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_assertion dct:description
      "[In this review, we focus on polymorphisms of the NFKB and NFKBI genes in relation to development of common inflammatory diseases including ulcerative colitis (UC), Crohn's disease (CD), rheumatoid arthritis, systemic lupus erythematosus, psoriatic arthritis, giant cell arthritis, type 1 diabetes, multiple sclerosis, celiac disease, and Parkinson's disease, as well as susceptibility of several cancers, such as oral squamous cell carcinoma, colorectal cancer (CRC), hepatocellular carcinoma, breast cancer and myeloma.]. 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:17701919;
    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:NP196299.RAAHDc7RS3panhZre58li8hbZk9FJMFa4Q3JLBR5l_X1s130_publicationInfo {
  this: dct:created "2014-10-02T12:33:48+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}