@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE> .
@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:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_head {
  this: np:hasAssertion dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_assertion ;
    np:hasProvenance dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_provenance ;
    np:hasPublicationInfo dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_assertion a np:Assertion .
  dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_provenance a np:Provenance .
  dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_assertion {
  miriam-gene:9260 a ncit:C16612 .
  lld:C0021345 a ncit:C7057 .
  dgn-gda:DGNe7b2237a3aff22451b86c0a23ea80e15 sio:SIO_000628 miriam-gene:9260 , lld:C0021345 ;
    a sio:SIO_001121 .
}
dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_provenance {
  dgn-np:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_assertion dcterms:description "[We analysed the 30-bp deletion and the single-base mutations of the LMP-1 gene in 13 spontaneously established lymphoblastoid cell lines (LCLs) from peripheral blood mononuclear cells of three healthy children, four patients with EBV-unrelated acute febrile illnesses, three patients with infectious mononucleosis (IM), and three patients with chronic active EBV infection (CEBV), and six frozen samples from four patients with CEBV and two patients with EBV-associated hemophagocytic syndrome (EBV-AHS).]. 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:8875994 ;
    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:NP234089.RA9oPZZ3e72KjZ0Z1oye00WYR2PdIIGmXpHCQ9b4ryTlE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:11+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" .
}