@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac> .
@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 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:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_head {
  this: np:hasAssertion dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_assertion;
    np:hasProvenance dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_provenance;
    np:hasPublicationInfo dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_assertion a np:Assertion .
  
  dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_provenance a np:Provenance .
  
  dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN3a9463a3d741d1031f49877345666337 sio:SIO_000628 miriam-gene:3133, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_provenance {
  dgn-np:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_assertion dct:description
      "[Because the pathogenesis of retinopathy is likely to be the same in IDDM and NIDDM, NIDDM subjects with retinopathy would be the ideal population to study for an association with MHC markers.]. 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:9157089;
    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:NP356655.RADXBB41PiYR6RAU7Qhlsop0JOTdYI7bCo3WlB-iZ4yac130_publicationInfo {
  this: dct:created "2014-10-02T12:35:29+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}