@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M> .
@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/v3.0.0/void/> .

dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_head {
  this: np:hasAssertion dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_assertion;
    np:hasProvenance dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_provenance;
    np:hasPublicationInfo dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_assertion a np:Assertion .
  
  dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_provenance a np:Provenance .
  
  dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_assertion {
  miriam-gene:723961 a ncit:C16612 .
  
  lld:C0271689 a ncit:C7057 .
  
  dgn-gda:DGN0e1e2bdc6a7fa5c9bcc5ef69507fd845 sio:SIO_000628 miriam-gene:723961, lld:C0271689;
    a sio:SIO_001121 .
}

dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_provenance {
  dgn-np:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_assertion dcterms:description
      "[Only a minority of cases of type 2 diabetes are caused by single gene defects such as maturity onset diabetes of the young (MODY), syndrome of insulin resistance (insulin receptor defect) and maternally inherited diabetes and deafness (mitochondrial gene defect).]. 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:14748467;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP1007834.RA-l7THAqz022XOKnvxYSpVloTZbtpNFEJ7vaf_rZ-69M130_publicationInfo {
  this: dcterms:created "2015-08-25T14:48:04+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}