@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0> .
@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:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_head {
  this: np:hasAssertion dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_assertion;
    np:hasProvenance dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_provenance;
    np:hasPublicationInfo dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_assertion a np:Assertion .
  
  dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_provenance a np:Provenance .
  
  dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_assertion {
  miriam-gene:50943 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN5633ae21b8fd6570eb45f280216ee0eb sio:SIO_000628 miriam-gene:50943, lld:C0003873;
    a sio:SIO_001121 .
}

dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_provenance {
  dgn-np:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_assertion dcterms:description
      "[The aim of this study was to assess the possible association of the functional (GT)(n) microsatellite polymorphism in the FOXP3 gene with predisposition to several autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), ulcerative colitis (UC), Crohn's disease, and celiac disease.]. 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:16216670;
    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:NP644594.RA_G1ArQjQHPPw_T7LmAFR7ylrrPbFKUo7_YZkyQ4_NK0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:28+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" .
}