@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM> .
@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:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_head {
  this: np:hasAssertion dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_assertion ;
    np:hasProvenance dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_provenance ;
    np:hasPublicationInfo dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_assertion a np:Assertion .
  dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_provenance a np:Provenance .
  dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_assertion {
  miriam-gene:6352 a ncit:C16612 .
  lld:C0027765 a ncit:C7057 .
  dgn-gda:DGN39454d761b1bc6bfba41e3e5969eadea sio:SIO_000628 miriam-gene:6352 , lld:C0027765 ;
    a sio:SIO_001121 .
}
dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_provenance {
  dgn-np:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_assertion dcterms:description "[As VE is a neurological disease characterized by the inflammatory reactions systematically observed in the spinocerebellar fluid and in the brain tissue of deceased patients, we examined 17 single nucleotide polymorphisms (SNPs) across seven inflammation-related candidate gene regions, including chemokine receptors type 2 and 5 (CCR2/CCR5), interferon-gamma (IFN-gamma), interleukin-4 (IL-4), IL-6, IL-10, stromal cell-derived factor (SDF) and chemokine regulated upon activation, normal T-cell expressed and presumably secreted (RANTES).]. 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:15182325 ;
    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:NP367636.RAqEnpYr9ldFiCX0ty4DqhOf3iisRd2WfsKl2SdmgnrpM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:35+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> ;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
}