@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_head {
  this: np:hasAssertion dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_assertion;
    np:hasProvenance dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_provenance;
    np:hasPublicationInfo dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_assertion a np:Assertion .
  
  dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_provenance a np:Provenance .
  
  dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_assertion {
  miriam-gene:6324 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN2eae7a8371230f700d78eca725b391e0 sio:SIO_000628 miriam-gene:6324, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_provenance {
  dgn-np:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_assertion dcterms:description
      "[To further examine the involvement of homozygous SCN1B mutations in the etiology of Dravet syndrome, we performed mutational analyses on SCN1B in 286 patients with epileptic disorders, including 67 patients with Dravet syndrome who have been negative for SCN1A and SCN2A mutations.]. 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:23148524;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP682630.RAr8j39eNIie7CFNpV8M32wKID8icLuQDBanbHzvRWA04130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:31+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}