@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs> .
@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:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_head {
  this: np:hasAssertion dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_assertion ;
    np:hasProvenance dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_provenance ;
    np:hasPublicationInfo dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_assertion a np:Assertion .
  dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_provenance a np:Provenance .
  dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_assertion {
  miriam-gene:920 a ncit:C16612 .
  lld:C0021053 a ncit:C7057 .
  dgn-gda:DGNfc89266386c5beb4f4d0646e2852dd31 sio:SIO_000628 miriam-gene:920 , lld:C0021053 ;
    a sio:SIO_001121 .
}
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_provenance {
  dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_assertion dcterms:description "[Genetic data, among others, suggest that viral infections are implicated and that natural killer effector pathways are important in the pathogenesis of CD, but most prominently these data converge with existing immunological findings that CD is primarily a T cell-mediated immune disorder in which CD4(+) T cells that recognize gluten peptides in the context of major histocompatibility class II molecules play a central role.]. 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:21219178 ;
    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:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:59+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" .
}