@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk> .
@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:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_head {
  this: np:hasAssertion dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_assertion;
    np:hasProvenance dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_provenance;
    np:hasPublicationInfo dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_assertion a np:Assertion .
  
  dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_provenance a np:Provenance .
  
  dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  
  lld:C0043117 a ncit:C7057 .
  
  dgn-gda:DGN113711d87e66e680d6c02a752cf037dc sio:SIO_000628 miriam-gene:1493, lld:C0043117;
    a sio:SIO_001121 .
}

dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_provenance {
  dgn-np:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_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;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:12555221;
    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:NP563723.RAZ7sKZxFZ0RTrRh6fcIa4uMyribu_OABRTkK681WWguk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:40+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" .
}