@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY> .
@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:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_head {
  this: np:hasAssertion dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_assertion;
    np:hasProvenance dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_provenance;
    np:hasPublicationInfo dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_assertion a np:Assertion .
  
  dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_provenance a np:Provenance .
  
  dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGNcc0d51008527bf8806a724b1eaf76dd0 sio:SIO_000628 miriam-gene:1636, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_provenance {
  dgn-np:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_assertion dcterms:description
      "[Multiple regression analysis showed that the effect of the ACE genotype was explained by its influence on serum ACE activity and that the only other significant determinants of the risk of severe hypoglycaemia were the degree of hypoglycaemia awareness, b-cell function, and duration of diabetes of more than 20 years.]. 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:11418149;
    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:NP294620.RAu0ik3K4UD9KX2tE3weN161vCMRqIq7yTaXjTNIEmmbY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}