@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE> .
@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:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_head {
  this: np:hasAssertion dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_assertion;
    np:hasProvenance dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_provenance;
    np:hasPublicationInfo dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_assertion a np:Assertion .
  
  dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_provenance a np:Provenance .
  
  dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN8f9b0f2fdf0603ff486d94576785bc02 sio:SIO_000628 miriam-gene:1493, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_provenance {
  dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_assertion dcterms:description
      "[The observed decrease in the frequency of GG genotype in the breast cancer patients is contrary to the frequently reported increase of GG genotype in autoimmune diseases. In addition, the data implies that polymorphism of ctla-4 exon 1 contributes in tumor progression.]. 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:15218356;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}