@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4> .
@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:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_head {
  this: np:hasAssertion dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_assertion;
    np:hasProvenance dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_provenance;
    np:hasPublicationInfo dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_assertion a np:Assertion .
  
  dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_provenance a np:Provenance .
  
  dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_assertion {
  miriam-gene:4790 a ncit:C16612 .
  
  lld:C0024305 a ncit:C7057 .
  
  dgn-gda:DGNaa440baf2f7c2154e78eedc5323d5dbd sio:SIO_000628 miriam-gene:4790, lld:C0024305;
    a sio:SIO_001122 .
}

dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_provenance {
  dgn-np:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_assertion dcterms:description
      "[we provide additional evidence for the role of genetic variation in TNF and LTA SNPs and haplotypes with risk of NHL and also provide some of the first preliminary evidence for an association of genetic variation in NFKB1, a downstream target of TNF sig]. 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:18990758;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP69050.RA6R5JNVYvww3aevF_usBW1K8u7_k29sN9Sh8tXeXaUN4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:33+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" .
}