@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4> .
@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:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_head {
  this: np:hasAssertion dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_assertion;
    np:hasProvenance dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_provenance;
    np:hasPublicationInfo dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_assertion a np:Assertion .
  
  dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_provenance a np:Provenance .
  
  dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_assertion {
  miriam-gene:6323 a ncit:C16612 .
  
  lld:C0036572 a ncit:C7057 .
  
  dgn-gda:DGN5c9487cad5a534d5053f6fa63603dc35 sio:SIO_000628 miriam-gene:6323, lld:C0036572;
    a sio:SIO_001121 .
}

dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_provenance {
  dgn-np:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_assertion dcterms:description
      "[The purpose of this study is to correlate different types of SCN1A mutations and (1) seizure control, (2) occurrence of convulsive status epilepticus (cSE), and (3) the presence of crouch gait in adult 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:22780858;
    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:NP405447.RAY4cebwoLOaWfK59ld1fKZpMIe3BSbazXMXjDD9rZYS4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:01+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" .
}