@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE> .
@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:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_head {
  this: np:hasAssertion dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_assertion;
    np:hasProvenance dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_provenance;
    np:hasPublicationInfo dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_assertion a np:Assertion .
  
  dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_provenance a np:Provenance .
  
  dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_assertion {
  miriam-gene:26191 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGN90c887ff49c472793dab01950fabbc7c sio:SIO_000628 miriam-gene:26191, lld:C0003873;
    a sio:SIO_001121 .
}

dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_provenance {
  dgn-np:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_assertion dcterms:description
      "[To determine whether association of this variant (PTPN22 1858T) with RA is reproducible and is also observed in another autoimmune condition, Crohn's disease, we investigated the association between the PTPN22 1858T allele and RA and Crohn's disease in a Canadian population.]. 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:15986374;
    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:NP198339.RAYCGK_7lXttLWtLu0YJc71ikq9uZChsmoXkxp9EaT2TE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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" .
}