@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0> .
@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:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_head {
  this: np:hasAssertion dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_assertion;
    np:hasProvenance dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_provenance;
    np:hasPublicationInfo dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_assertion a np:Assertion .
  
  dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_provenance a np:Provenance .
  
  dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  
  lld:C0339143 a ncit:C7057 .
  
  dgn-gda:DGN2f9672fff50b8444d7d194b4491a3cfe sio:SIO_000628 miriam-gene:1493, lld:C0339143;
    a sio:SIO_001121 .
}

dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_provenance {
  dgn-np:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_assertion dcterms:description
      "[We analyzed the A(49)G exon 1 CTLA-4 gene polymorphism in 99 unrelated Polish patients with GD, of whom 50 had clinically evident GO (NOSPECS class III and higher), and 154 matched healthy subjects from the Lower Silesia region.]. 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:15507878;
    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:NP326609.RAv7LW7smbyJINkcftdF0Vc0MKL1larZ2qLDm4_S8kSt0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:11+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" .
}