@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc> .
@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:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_head {
  this: np:hasAssertion dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_assertion;
    np:hasProvenance dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance;
    np:hasPublicationInfo dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_assertion a np:Assertion .
  
  dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance a np:Provenance .
  
  dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_assertion {
  miriam-gene:9211 a ncit:C16612 .
  
  lld:C0014556 a ncit:C7057 .
  
  dgn-gda:DGN97f80c6b6ff453d3a4d1cbdc2230593e sio:SIO_000628 miriam-gene:9211, lld:C0014556;
    a sio:SIO_001121 .
}

dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_provenance {
  dgn-np:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_assertion dcterms:description
      "[Mutation of LGI1 gene has been identified in familial lateral temporal lobe epilepsy while mutations of genes which encode sodium channels and GABAA receptors have been reported in generalized epilepsy with febrile seizure plus.]. 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:17981785;
    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:NP619468.RAFh5Wo0D0D7nc5RT7FofOoxx3B2_JQuEYzfDStYNEYOc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:14+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" .
}