@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs> .
@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:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_head {
  this: np:hasAssertion dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_assertion;
    np:hasProvenance dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_provenance;
    np:hasPublicationInfo dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_assertion a np:Assertion .
  
  dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_provenance a np:Provenance .
  
  dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_assertion {
  miriam-gene:1137 a ncit:C16612 .
  
  lld:C0270853 a ncit:C7057 .
  
  dgn-gda:DGN8c64231bf7b08cd3110bae955afc4ffd sio:SIO_000628 miriam-gene:1137, lld:C0270853;
    a sio:SIO_001121 .
}

dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_provenance {
  dgn-np:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_assertion dcterms:description
      "[Susceptibility genes for two syndromes of idiopathic generalized epilepsies, the benign familial neonatal convulsions and juvenile myoclonic epilepsy, have been assigned to the chromosomal regions 20q13 (EBN1), 8q24 (EBN2) and 6p21 (EJM1).]. 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:8796880;
    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:NP1357070.RAlbiAU_zMSbCu9Qf8m0Q_WwcO_7ym0MfnvEq57UKFfNs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:01+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: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" .
}