@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE> .
@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:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_head {
  this: np:hasAssertion dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_assertion ;
    np:hasProvenance dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_provenance ;
    np:hasPublicationInfo dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_assertion a np:Assertion .
  dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_provenance a np:Provenance .
  dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  lld:C0004943 a ncit:C7057 .
  dgn-gda:DGN6c9a56ab9452d598a0c5949b21a87774 sio:SIO_000628 miriam-gene:1493 , lld:C0004943 ;
    a sio:SIO_001121 .
}
dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_provenance {
  dgn-np:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_assertion dcterms:description "[Although our understanding of the role of the CTLA4 gene and its protein product in BD is incomplete, these results suggest that single nucleotide polymorphisms of the promoter and exon regions in the CTLA4 gene are candidates that predispose to BD and that sCTLA4 may be related to the immunological abnormalities and disease expressions associated with BD.]. 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:19563524 ;
    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:NP197363.RAlXoUY9U4tH0ttgUVG-oHG5QB6ZOXaEnXzlocce2pylE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}