@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0> .
@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:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_head {
  this: np:hasAssertion dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_assertion;
    np:hasProvenance dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_provenance;
    np:hasPublicationInfo dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_assertion a np:Assertion .
  
  dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_provenance a np:Provenance .
  
  dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C0020456 a ncit:C7057 .
  
  dgn-gda:DGN24b6684b0eb61bdb7e171d07236a132e sio:SIO_000628 miriam-gene:3630, lld:C0020456;
    a sio:SIO_001121 .
}

dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_provenance {
  dgn-np:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_assertion dcterms:description
      "[The authors present here the clinical, anatomic, and endocrine-metabolic studies of three patients, with a view toward careful delineation of the syndrome and further characterization of the metabolic defect.The most striking and consistent metabolic derangements present in all of these patients were fasting hypoglycemia (less than 20 mg/dL), postprandial hyperglycemia (more than 250 mg/dL), marked hyperinsulinemia (more than 2000 μU/mL), and severe insulin resistance (less than a 20 percent decrease in blood sugar with 0.3 to 1.0 U/kg of regular insulin IV).]. 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:7154104;
    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:NP163321.RAx-T8fZlUGDCr6At6lAnThQ_rKxSH9lr_kHpmOWBwbi0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:28+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" .
}