@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_head {
   this: np:hasAssertion dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion ;
    np:hasProvenance dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_provenance ;
    np:hasPublicationInfo dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion a np:Assertion .
  dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_provenance a np:Provenance .
  dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion {
   miriam-gene:3133 a ncit:C16612 .
  lld:C0024141 a ncit:C7057 .
  dgn-gda:DGN5dde4f66f86847963ac99fead0222c10 sio:SIO_000628 miriam-gene:3133 , lld:C0024141 ;
    a sio:SIO_001121 .
}
dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_provenance {
   dgn-np:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_assertion dcterms:description "[We genotyped a panel of 1,472 SNPs to capture the common genomic variation across the 3.44 megabase (Mb) classic MHC region in 10,576 DNA samples derived from patients with systemic lupus erythematosus, Crohn's disease, ulcerative colitis, rheumatoid arthritis, myasthenia gravis, selective IgA deficiency, multiple sclerosis, and appropriate control samples.]. 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:19846760 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP770872.RADp26wHuIWOBCnKGmWeyiiQtweVsTkBPNGiJ8NvNlqaI130_publicationInfo {
   this: dcterms:created "2016-05-13T12:47:34+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}