@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c> .
@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:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_head {
  this: np:hasAssertion dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_assertion;
    np:hasProvenance dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_provenance;
    np:hasPublicationInfo dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_assertion a np:Assertion .
  
  dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_provenance a np:Provenance .
  
  dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_assertion {
  miriam-gene:3767 a ncit:C16612 .
  
  lld:C0158981 a ncit:C7057 .
  
  dgn-gda:DGNeee369ad107a2275f0e86f4990d4e276 sio:SIO_000628 miriam-gene:3767, lld:C0158981;
    a sio:SIO_001121 .
}

dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_provenance {
  dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_assertion dcterms:description
      "[Our report suggests that screening for KCNJ11 mutations is appropriate in patients diagnosed with neonatal diabetes as it provides valuable information concerning possible course of the disease and choice of treatment.]. 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:20401705;
    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:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:50+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" .
}