@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI> .
@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:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_head {
  this: np:hasAssertion dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_assertion;
    np:hasProvenance dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_provenance;
    np:hasPublicationInfo dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_assertion a np:Assertion .
  
  dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_provenance a np:Provenance .
  
  dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_assertion {
  miriam-gene:4068 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN7288e76e853a98978b0a80bc79a641f2 sio:SIO_000628 miriam-gene:4068, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_provenance {
  dgn-np:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_assertion dcterms:description
      "[The discovery that a single-nucleotide polymorphism (SNP) in lymphoid tyrosine phosphatase (LYP), encoded by the PTPN22 gene, is associated with type 1 diabetes (T1D) has now been verified by numerous studies and has been expanded to rheumatoid arthritis, juvenile rheumatoid arthritis (JRA), systemic lupus erythematosus, Graves' disease, generalized vitiligo and other human autoimmune diseases.]. 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:17729039;
    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:NP774338.RA2dw5GbYL95CSdUkoJ6cNNvSpclD_TTh2LL8bw2LMGlI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:48+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" .
}