@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I> .
@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:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_head {
  this: np:hasAssertion dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_assertion;
    np:hasProvenance dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_provenance;
    np:hasPublicationInfo dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_assertion a np:Assertion .
  
  dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_provenance a np:Provenance .
  
  dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_assertion {
  miriam-gene:8874 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGN7decdf9d4b07627b9a343ca87a1b2563 sio:SIO_000628 miriam-gene:8874, lld:C0010054;
    a sio:SIO_001121 .
}

dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_provenance {
  dgn-np:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_assertion dcterms:description
      "[The deletion variant allele of the NFKB1 - 94ins/delATTG promoter polymorphism leads to lower transcript levels of the p50 subunit, and the variant allele has been associated with the risk of several inflammatory diseases as well as coronary heart disease where inflammation is important in the pathogenesis.]. 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:23671649;
    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:NP885306.RArTOJd2Tcwhe6d5nOLNJdA0W5qkoBxPLr4StHy7dGF7I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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" .
}