@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ> .
@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:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_head {
  this: np:hasAssertion dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_assertion;
    np:hasProvenance dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_provenance;
    np:hasPublicationInfo dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_assertion a np:Assertion .
  
  dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_provenance a np:Provenance .
  
  dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_assertion {
  miriam-gene:6323 a ncit:C16612 .
  
  lld:C3501832 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_provenance {
  dgn-np:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_assertion dcterms:description
      "[To clarify the genotypic differences in this group of epilepsies, we searched for SCN1A abnormalities in 25 patients with SMEI and 10 with ICEGTC, together with the family members of 15 patients.]. 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:12566275;
    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:NP856076.RAXW1LihOhQmzif309oqshKIHVldAYsFu5LAun9eyXOIQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}