@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U> .
@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:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_head {
   this: np:hasAssertion dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_assertion ;
    np:hasProvenance dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_provenance ;
    np:hasPublicationInfo dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_assertion a np:Assertion .
  dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_provenance a np:Provenance .
  dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_assertion {
   miriam-gene:26191 a ncit:C16612 .
  lld:C1304470 a ncit:C7057 .
  dgn-gda:DGN839d056a27b053c28fc97ba93c290068 sio:SIO_000628 miriam-gene:26191 , lld:C1304470 ;
    a sio:SIO_001121 .
}
dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_provenance {
   dgn-np:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_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:NP790172.RAhSrjN_JHAyZib7VKQtYpsVjpaTGdVk_XIZJ_aNmOk8U130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:05+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" .
}