@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o> .
@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:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_head {
  this: np:hasAssertion dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_assertion;
    np:hasProvenance dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_provenance;
    np:hasPublicationInfo dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_assertion a np:Assertion .
  
  dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_provenance a np:Provenance .
  
  dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_assertion {
  miriam-gene:6657 a ncit:C16612 .
  
  lld:C0015397 a ncit:C7057 .
  
  dgn-gda:DGN66a1cf072b081313062ee416a1a1845e sio:SIO_000628 miriam-gene:6657, lld:C0015397;
    a sio:SIO_001121 .
}

dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_provenance {
  dgn-np:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_assertion dcterms:description
      "[We searched for SOX2 mutation in 24 patients with typical hippocampal sclerosis and for common variations in SOX2 in 655 patients without eye disease but with epilepsy, including 91 patients with febrile seizures, 93 with hippocampal sclerosis, and 258 with temporal lobe epilepsy.]. 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:16529618;
    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:NP315529.RAB0pPGyfvpfWnbVSwdbvSDZTGDSxYv4YehLSNptBWN9o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
}