@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU> .
@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:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_head {
  this: np:hasAssertion dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_assertion ;
    np:hasProvenance dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_provenance ;
    np:hasPublicationInfo dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_assertion a np:Assertion .
  dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_provenance a np:Provenance .
  dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  lld:C0042900 a ncit:C7057 .
  dgn-gda:DGN3e5c86685d9d78ecbfb7f90fed3fa545 sio:SIO_000628 miriam-gene:1493 , lld:C0042900 ;
    a sio:SIO_001121 .
}
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_provenance {
  dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_assertion dcterms:description "[CTLA-4 gene microsatellite polymorphisms were determined for 74 vitiligo patients (53 without any autoimmune disorder; 21 with one or more autoimmune disease) and 173 healthy controls, who had no clinical evidence of either vitiligo or any other autoimmune disorder, by polymerase chain reaction amplification of genomic DNA and resolution of the products on polyacrylamide sequencing gels.]. 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:10215771 ;
    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:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:35+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" .
}