@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss> .
@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:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_head {
  this: np:hasAssertion dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_assertion;
    np:hasProvenance dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_provenance;
    np:hasPublicationInfo dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_assertion a np:Assertion .
  
  dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_provenance a np:Provenance .
  
  dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_assertion {
  miriam-gene:6833 a ncit:C16612 .
  
  lld:C0342276 a ncit:C7057 .
  
  dgn-gda:DGN4afe4c2609e6baf0e7de86d82f1236c6 sio:SIO_000628 miriam-gene:6833, lld:C0342276;
    a sio:SIO_001121 .
}

dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_provenance {
  dgn-np:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_assertion dcterms:description
      "[Finally, the example of single gene diabetes, particularly HNF1A MODY and permanent neonatal diabetes associated with the KCNJ11 and ABCC8 genes, all efficiently controlled on sulfonylurea, inspires us to continue the efforts to tailor individual treatment for T2DM patients.]. 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:22996131;
    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:NP302481.RA_kBuT9bAjYPFFhmZUDIFJqHHtSpsYd6w9srvOv3Chss130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:54+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" .
}