@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_head {
  this: np:hasAssertion dgn-np:NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_assertion ;
    np:hasProvenance dgn-np:NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance ;
    np:hasPublicationInfo dgn-np:NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_assertion {
  miriam-gene:115352 a ncit:C16612 .
  lld:C0011854 a ncit:C7057 .
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dgn-np:NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance {
  dgn-np:NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_assertion dcterms:description "[We analyzed the same four 5' FCRL3 single nucleotide polymorphism markers, together with three additional exonic single nucleotide polymorphisms in the FCRL3 gene, in cohorts of white Caucasians with Graves' disease (n = 625), type 1 diabetes (n = 279), autoimmune Addison's disease (AAD; n = 200), and RA (n = 769).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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  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:NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:11+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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