@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_head {
  this: np:hasAssertion dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_assertion;
    np:hasProvenance dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_provenance;
    np:hasPublicationInfo dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_assertion a np:Assertion .
  
  dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_provenance a np:Provenance .
  
  dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  
  lld:C0007570 a ncit:C7057 .
  
  dgn-gda:DGN02f6e2fc4e0c5097c69f3f17d80f239b sio:SIO_000628 miriam-gene:1493, lld:C0007570;
    a sio:SIO_001122 .
}

dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_provenance {
  dgn-np:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_assertion dcterms:description
      "[Our data show a significant effect of the CTLA4 CT60G allele at the homozygous state on the risk of developing AITD in children with CD and suggest that the reported association of the CTLA4 CT60 A/G polymorphism with CD is limited to the subgroup of patients who are or will be complicated with AITD.]. 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:18929517;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP55965.RAvS97h7Uh0PTRsH33V_ZnXoKxsP6exoFFMgJOR0cm8PM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:10+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}