@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk> .
@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:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_head {
   this: np:hasAssertion dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_assertion ;
    np:hasProvenance dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_provenance ;
    np:hasPublicationInfo dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_assertion a np:Assertion .
  dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_provenance a np:Provenance .
  dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_assertion {
   miriam-gene:4217 a ncit:C16612 .
  lld:C0024305 a ncit:C7057 .
  dgn-gda:DGN245f404a4fdd4c6a34f3e02cf83d2679 sio:SIO_000628 miriam-gene:4217 , lld:C0024305 ;
    a sio:SIO_001121 .
}
dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_provenance {
   dgn-np:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_assertion dcterms:description "[Our results suggest that genetic variation in genes associated with immune response (TRAF1, RIPK3, BAT2, and TLR6), mitogen-activated protein kinase (MAPK) signaling (MAP3K5, DUSP2, and CREB1), lymphocyte trafficking and migration (B3GNT3, SELPLG, and LSP1), and coagulation pathways (FGG and ITGB3) may be important in the etiology of NHL, and should be prioritized in replication studies.]. 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:17827388 ;
    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:NP598929.RAl19cFQ_XQshuZvrymjmm8OVFhNFfyOSYT_Q9I5_deSk130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:00+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" .
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}