@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0> .
@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:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_head {
  this: np:hasAssertion dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_assertion ;
    np:hasProvenance dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_provenance ;
    np:hasPublicationInfo dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_assertion a np:Assertion .
  dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_provenance a np:Provenance .
  dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  lld:C0018213 a ncit:C7057 .
  dgn-gda:DGN71b0790b61d8429f91068143213a9621 sio:SIO_000628 miriam-gene:3133 , lld:C0018213 ;
    a sio:SIO_001121 .
}
dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_provenance {
  dgn-np:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_assertion dcterms:description "[We have now demonstrated, on the basis of disease-associated MHC haplotypes (A1, Cw3, B8, DR3 and fragments thereof) from 38 families in which more than one member had Graves' disease compared with MHC haplotypes from 56 healthy families, that the risk was highest with the DR locus (relative risk for A1, B8, DR3 = 2.3, for B8, DR3 = 5.3, and for DR3 = 6.8).]. 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:3485758 ;
    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:NP402773.RAT7t2LpOXS9DzRCOEU1WQoaRmAd8mLlKBb6CbytWpkN0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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" .
}