@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM> .
@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:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_head {
  this: np:hasAssertion dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_assertion ;
    np:hasProvenance dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_provenance ;
    np:hasPublicationInfo dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_assertion a np:Assertion .
  dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_provenance a np:Provenance .
  dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_assertion {
  miriam-gene:2212 a ncit:C16612 .
  lld:C0024305 a ncit:C7057 .
  dgn-gda:DGNeec5223fb61c2da979105412d026ac42 sio:SIO_000628 miriam-gene:2212 , lld:C0024305 ;
    a sio:SIO_001122 .
}
dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_provenance {
  dgn-np:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_assertion dcterms:description "[common variants in genes influencing proinflammatory and innate immune responses were associated with non-Hodgkin lymphoma risk overall and their effects could vary by subtype. Our results require replication but potentially provide important clues for investigating common genetic variants as susceptibility factors and in disease outcomes, treatment responses, and immunotherapy targets. (Cancer Res 2006; 66(19): 9771-80).]. 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:17018637 ;
    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:NP64547.RA0qaqUmXf_3DvK7YmsVO-EwF4RzRUtJkseo9UBThSimM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}