@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE> .
@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:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_head {
  this: np:hasAssertion dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_assertion;
    np:hasProvenance dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_provenance;
    np:hasPublicationInfo dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_assertion a np:Assertion .
  
  dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_provenance a np:Provenance .
  
  dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_assertion {
  miriam-gene:59271 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGNadb55b64c815ef32e1e41e63459c47e0 sio:SIO_000628 miriam-gene:59271, lld:C0011849;
    a sio:SIO_001121 .
}

dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_provenance {
  dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_assertion dcterms:description
      "[The frequency of the whole haplotype Cw5, B18, BfF1, DR3 and of its segment BfF1, DR3, and the strength of the gametic associations between these alleles were much higher in IDD patients than in non-diabetic controls, irrespective of the age of onset of their diabetes.]. 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:6607851;
    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:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:03+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" .
}