@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o> .
@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/v4.0.0/void/> .

dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_head {
  this: np:hasAssertion dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_assertion;
    np:hasProvenance dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_provenance;
    np:hasPublicationInfo dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_assertion a np:Assertion .
  
  dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_provenance a np:Provenance .
  
  dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_assertion {
  miriam-gene:3106 a ncit:C16612 .
  
  lld:C0038325 a ncit:C7057 .
  
  dgn-gda:DGN0eb6a95b6e7927efd32aba1e348b0015 sio:SIO_000628 miriam-gene:3106, lld:C0038325;
    a sio:SIO_001121 .
}

dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_provenance {
  dgn-np:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_assertion dcterms:description
      "[Although the current studies associating particular genes and their variants with seizure control or adverse events have inherent weaknesses and have not provided unifying conclusions, several results, for example that Asian patients with a particular HLA allele, HLA-B*1502, are at a higher risk for Stevens-Johnson syndrome when using carbamazepine, are helpful to increase our knowledge how genetic variation affects the treatment of 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:18627414;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP682176.RAtb6BB8JzaoKOw7rrvkNAOmCwDDSazRF5s2lKIz8EP5o130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:54+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}