@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk> .
@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:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_head {
  this: np:hasAssertion dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_assertion;
    np:hasProvenance dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_provenance;
    np:hasPublicationInfo dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_assertion a np:Assertion .
  
  dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_provenance a np:Provenance .
  
  dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_assertion {
  miriam-gene:3401 a ncit:C16612 .
  
  lld:C0011854 a ncit:C7057 .
  
  dgn-gda:DGNb6703269beb4545b356b8f58ed77034d sio:SIO_000628 miriam-gene:3401, lld:C0011854;
    a sio:SIO_001121 .
}

dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_provenance {
  dgn-np:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_assertion dcterms:description
      "[Of the 20 genomic intervals implicated for the risk to develop T1D, the major histocompatibility complex (MHC) region on chromosome 6p21.31 (IDDM1) has been the major contributor, followed by 5' regulatory region of the insulin (INS) gene on chromosome 11p15.5 (IDDM2).]. 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:15245369;
    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:NP293522.RA_WprGTxY4c_F0rWEk3swoFb1htUVvpl0fKtMVEMqvLk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}