@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos> .
@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:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_head {
  this: np:hasAssertion dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_assertion;
    np:hasProvenance dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_provenance;
    np:hasPublicationInfo dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_assertion a np:Assertion .
  
  dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_provenance a np:Provenance .
  
  dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_assertion {
  miriam-gene:10984 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGNcd3ec3a278f1186a83f28cc16d799d61 sio:SIO_000628 miriam-gene:10984, lld:C0011849;
    a sio:SIO_001121 .
}

dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_provenance {
  dgn-np:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_assertion dcterms:description
      "[We demonstrate that CDKN1C, KCNQ1, and KCNQ1OT1 are most likely to mediate diabetes susceptibility at the KCNQ1 locus and identify temporal differences in imprinting status and methylation effects, suggesting that diabetes risk effects may be mediated in early development.]. 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:23139357;
    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:NP825081.RAPFcxG6ZNJ8eHxX3bYQKeXpFjaeMqG5aRsbVwFPXAwos130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:25+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" .
}