@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw> .
@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:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_head {
   this: np:hasAssertion dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_assertion ;
    np:hasProvenance dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_provenance ;
    np:hasPublicationInfo dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_assertion a np:Assertion .
  dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_provenance a np:Provenance .
  dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_assertion {
   miriam-gene:3669 a ncit:C16612 .
  lld:C0026769 a ncit:C7057 .
  dgn-gda:DGN2a50cd5360b5e112f2ab1bebe65b0fdd sio:SIO_000628 miriam-gene:3669 , lld:C0026769 ;
    a sio:SIO_001121 .
}
dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_provenance {
   dgn-np:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_assertion dcterms:description "[Here we use polychromatic flow cytometry to show that differences in surface expression of the human interleukin-2 (IL-2) receptor alpha (IL2RA, or CD25) protein are restricted to particular immune cell types and correlate with several haplotypes in the IL2RA region that have previously been associated with two autoimmune diseases, type 1 diabetes (T1D) and multiple sclerosis.]. 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:19701192 ;
    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:NP203950.RAUfFpsecevQo00X6Xm8wqRjwfN9CSttLVgYJX7rL6nWw130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:52+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> ;
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    pav:version "v2.1.0.0" .
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}