@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM> .
@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:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_head {
  this: np:hasAssertion dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_assertion;
    np:hasProvenance dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_provenance;
    np:hasPublicationInfo dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_assertion a np:Assertion .
  
  dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_provenance a np:Provenance .
  
  dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_assertion {
  miriam-gene:6323 a ncit:C16612 .
  
  lld:C1306587 a ncit:C7057 .
  
  dgn-gda:DGN3069a877d5c89b6c9d92e479e96934a2 sio:SIO_000628 miriam-gene:6323, lld:C1306587;
    a sio:SIO_001121 .
}

dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_provenance {
  dgn-np:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_assertion dcterms:description
      "[We analyzed the SCN1A gene in 87 patients with acute encephalopathy, consisting of 20 with acute necrotizing encephalopathy (ANE), 61 with acute encephalopathy with biphasic seizures and late reduced diffusion (AESD), and six with nonspecific (unclassified) acute encephalopathy.]. 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:22309220;
    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:NP411760.RAlORP43894DsylSk5ERwdTwBxPaCc3qiThjPwSyxasTM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:04+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" .
}