@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko> .
@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:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_head {
   this: np:hasAssertion dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_assertion ;
    np:hasProvenance dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_provenance ;
    np:hasPublicationInfo dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_assertion a np:Assertion .
  dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_provenance a np:Provenance .
  dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_assertion {
   miriam-gene:1861 a ncit:C16612 .
  lld:C0011849 a ncit:C7057 .
  dgn-gda:DGNa005a89331bf0c3a69767f9f6173ee53 sio:SIO_000628 miriam-gene:1861 , lld:C0011849 ;
    a sio:SIO_001121 .
}
dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_provenance {
   dgn-np:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_assertion dcterms:description "[This suggests that if all alleles are truly identical for the major A1, B8, DR3 haplotype (between A1 and DR3), with different alleles on nonconserved haplotypes without differential diabetes risk, then in this region of the genome DR3-DQ2 may be the primary polymorphisms of common haplotypes contributing to diabetes risk.]. 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:15919812 ;
    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:NP736999.RAOdPbW43IlhuavYz8cW86TqIOImgnUMg_ZPigL8uE6Ko130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:27+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" .
}