@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg> .
@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:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_head {
  this: np:hasAssertion dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_assertion;
    np:hasProvenance dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_provenance;
    np:hasPublicationInfo dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_assertion a np:Assertion .
  
  dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_provenance a np:Provenance .
  
  dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_assertion {
  miriam-gene:1137 a ncit:C16612 .
  
  lld:C0391957 a ncit:C7057 .
  
  dgn-gda:DGNc035b8b7b9b5bd500f3ca1352df3da3a sio:SIO_000628 miriam-gene:1137, lld:C0391957;
    a sio:SIO_001121 .
}

dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_provenance {
  dgn-np:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_assertion dcterms:description
      "[The alpha4-subunit gene (CHRNA4) of the neuronal nicotinic acetylcholine receptor (nAChR) subunit family has recently been identified in two families as the gene responsible for autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), a rare monogenic idiopathic epilepsy.]. 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:9921897;
    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:NP783585.RAloRAFdH5EXaiZpC5nozMLWRZskuifPItgtGfuLx3xpg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:54+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" .
}