@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0> .
@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:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_head {
  this: np:hasAssertion dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_assertion;
    np:hasProvenance dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_provenance;
    np:hasPublicationInfo dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_assertion a np:Assertion .
  
  dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_provenance a np:Provenance .
  
  dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_assertion {
  miriam-gene:84059 a ncit:C16612 .
  
  lld:C2931469 a ncit:C7057 .
  
  dgn-gda:DGN224e07e5c1b944afd75895da21c3b60e sio:SIO_000628 miriam-gene:84059, lld:C2931469;
    a sio:SIO_001121 .
}

dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_provenance {
  dgn-np:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_assertion dcterms:description
      "[Two apparent exceptions to this rule are the MASS1 gene, which is mutated in the Frings mouse model of audiogenic epilepsy, and the LGI1 gene, which is mutated in autosomal dominant partial epilepsy with auditory features (ADPEAF).]. 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:12095917;
    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:NP620966.RAiGIBJ9dOcwsR7ZTQXcd3TNTJiS7B02uqUHFaKrVoQv0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+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" .
}