@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y> .
@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:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_head {
   this: np:hasAssertion dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_assertion ;
    np:hasProvenance dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_assertion a np:Assertion .
  dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_provenance a np:Provenance .
  dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_assertion {
   miriam-gene:1109 a ncit:C16612 .
  lld:C0003864 a ncit:C7057 .
  dgn-gda:DGN33b4acb7e5a5e4a0042518f8dd43df0b sio:SIO_000628 miriam-gene:1109 , lld:C0003864 ;
    a sio:SIO_001121 .
}
dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_provenance {
   dgn-np:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_assertion dcterms:description "[Using a series of inbred rat strains involving various genetic backgrounds (DA, LEW, E3), and congenic MHC regions (a, u, f, n, c, d), we found that CXI induced arthritis (C(XI)IA) is associated with the RT1f haplotype in contrast to CII induced arthritis (C(II)IA), which is associated with the RT1a and RT1u haplotypes.]. 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:12126633 ;
    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:NP207672.RAtp5nCyp6FqL2GlKWzhcQmzA6TAyylpewWHIYY_gzp7Y130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:54+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" .
}