@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_head {
  this: np:hasAssertion dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_assertion;
    np:hasProvenance dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_provenance;
    np:hasPublicationInfo dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_assertion a np:Assertion .
  
  dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_provenance a np:Provenance .
  
  dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_assertion {
  miriam-gene:3767 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGNaad5e6c63934d22643c8903583e234f6 sio:SIO_000628 miriam-gene:3767, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_provenance {
  dgn-np:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_assertion dcterms:description
      "[They indicate testing for KCNJ11 mutations should be considered not only for neonatal diabetes but also for other forms of dominantly inherited diabetes with later onset, especially where these are associated with a low body mass index and low birth weight.]. 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:18544102;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP675866.RAESrT1gRYwy7NhnNZKZMpJXiLoZq-SJEil8uHO2FESaA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:51+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}