@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg> .
@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:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_head {
  this: np:hasAssertion dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_assertion;
    np:hasProvenance dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_provenance;
    np:hasPublicationInfo dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_assertion a np:Assertion .
  
  dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_provenance a np:Provenance .
  
  dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_assertion {
  miriam-gene:50987 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN6e724348c4536cd3800b0f7c6b2a0e98 sio:SIO_000628 miriam-gene:50987, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_provenance {
  dgn-np:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_assertion dcterms:description
      "[Since candidate genes for FPEVF (familial partial epilepsy with variable foci) have been mapped by linkage studies in the same cytogenetic band of chromosome 22 involved in the translocation, this case can be helpful to identify genes involved in this form 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:19539447;
    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:NP818316.RA_SDHYTLwmT6NV4CRNWpiTYfToC_hOsP_VMTEUZPGNXg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:21+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" .
}