@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go> .
@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:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_head {
  this: np:hasAssertion dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_assertion ;
    np:hasProvenance dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_provenance ;
    np:hasPublicationInfo dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_assertion a np:Assertion .
  dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_provenance a np:Provenance .
  dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_assertion {
  miriam-gene:3120 a ncit:C16612 .
  lld:C0277554 a ncit:C7057 .
  dgn-gda:DGN5cd20298b3322f07a3c1ee430757d7f3 sio:SIO_000628 miriam-gene:3120 , lld:C0277554 ;
    a sio:SIO_001121 .
}
dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_provenance {
  dgn-np:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_assertion dcterms:description "[Although in the vast majority of patients with celiac disease, the HLA-DQ(alpha1*0501, beta1*0201) heterodimer encoded by the alleles HLA-DQA1*0501 and HLA-DQB1*0201 seems to confer the primary disease susceptibility, it cannot be excluded that other genes contribute to disease susceptibility, as indicated by the difference in concordance rates between monozygotic twins and HLA identical siblings (70% vs. 30%).]. 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:8820404 ;
    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:NP209582.RAXCfCh5QUasjKfrDUHx5k1cur2U_TJNQYvJ33-7GF1Go130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:55+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" .
}