@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA> .
@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:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_head {
  this: np:hasAssertion dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_assertion;
    np:hasProvenance dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_provenance;
    np:hasPublicationInfo dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_assertion a np:Assertion .
  
  dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_provenance a np:Provenance .
  
  dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_assertion {
  miriam-gene:27319 a ncit:C16612 .
  
  lld:C0011854 a ncit:C7057 .
  
  dgn-gda:DGN93b921ddc0b0fc0aec2fa56c58f5fb92 sio:SIO_000628 miriam-gene:27319, lld:C0011854;
    a sio:SIO_001121 .
}

dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_provenance {
  dgn-np:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_assertion dcterms:description
      "[However, four DR4-DQ beta 3.2 haplotypes that lack DX alpha-TaqI-2.2kb were encountered, two of which are affected. These haplotypes suggest that the identification of the disease locus can be facilitated by the study of unusual haplotypes in which distinct IDDM-associated alleles occur separated from their neighbors of the standard genetic configurations.]. 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:2563360;
    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:NP1259381.RAH4SUWhwxxkQevvK-NpO2vRcgYM73FJtLwBZfzFmAWzA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:17+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" .
}