@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4> .
@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:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_head {
  this: np:hasAssertion dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_assertion;
    np:hasProvenance dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_provenance;
    np:hasPublicationInfo dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_assertion a np:Assertion .
  
  dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_provenance a np:Provenance .
  
  dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_assertion {
  miriam-gene:3786 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN4dd83563ac54184e1e6b0eb3e1fd8d21 sio:SIO_000628 miriam-gene:3786, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_provenance {
  dgn-np:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_assertion dcterms:description
      "[Mutations in two neuronal voltage-gated potassium channel genes (KCNQ2 and KCNQ3) have already been shown to cause epilepsy (BFNC), and we now tested the hypothesis that genetic variation in the KCNQ3 gene confers liability to common IGE subtypes.]. 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:10996506;
    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:NP295473.RAkF4Aq0aAaYtEc5mzmJmd82ufbHs5hxPWfmw_Umt3-K4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:59+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" .
}