@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP228990.RA1GlBtXSWB6oS8CaXZ-sDCl4vW0O-G9YhLJWFOJvQ7aI> .
@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#> .
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  this: np:hasAssertion dgn-np:NP228990.RA1GlBtXSWB6oS8CaXZ-sDCl4vW0O-G9YhLJWFOJvQ7aI130_assertion ;
    np:hasProvenance dgn-np:NP228990.RA1GlBtXSWB6oS8CaXZ-sDCl4vW0O-G9YhLJWFOJvQ7aI130_provenance ;
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  dgn-np:NP228990.RA1GlBtXSWB6oS8CaXZ-sDCl4vW0O-G9YhLJWFOJvQ7aI130_provenance a np:Provenance .
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}
dgn-np:NP228990.RA1GlBtXSWB6oS8CaXZ-sDCl4vW0O-G9YhLJWFOJvQ7aI130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  lld:C0023434 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP228990.RA1GlBtXSWB6oS8CaXZ-sDCl4vW0O-G9YhLJWFOJvQ7aI130_provenance {
  dgn-np:NP228990.RA1GlBtXSWB6oS8CaXZ-sDCl4vW0O-G9YhLJWFOJvQ7aI130_assertion dcterms:description "[In the present study we have examined the prevalence of the A and G alleles of the CTLA-4 gene in 50 patients with autoimmune hemolytic anemia (AIHA), of which 20 had idiopathic AIHA and 30 had AIHA and chronic lymphocytic leukemia (CLL), and in 60 patients with immune thrombocytopenic purpura (ITP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP228990.RA1GlBtXSWB6oS8CaXZ-sDCl4vW0O-G9YhLJWFOJvQ7aI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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