@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI> .
@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:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_head {
  this: np:hasAssertion dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_assertion;
    np:hasProvenance dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_provenance;
    np:hasPublicationInfo dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_assertion a np:Assertion .
  
  dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_provenance a np:Provenance .
  
  dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_assertion {
  miriam-gene:3767 a ncit:C16612 .
  
  lld:C1833104 a ncit:C7057 .
  
  dgn-gda:DGNc29825b17821c3963da7a69ef634f9a3 sio:SIO_000628 miriam-gene:3767, lld:C1833104;
    a sio:SIO_001121 .
}

dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_provenance {
  dgn-np:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_assertion dcterms:description
      "[Heterozygous activating mutations of KCNJ11 (Kir6.2) are the most common cause of permanent neonatal diabetes mellitus (NDM), and successful glycemic control has been obtained in several cases with oral sulfonylureas (SU).]. 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:23382304;
    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:NP216328.RAa8iAHUQSR64ICtkfQF7NOHJ7ACd9cbw5GFXOaqRKLlI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}