@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0> .
@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:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_head {
  this: np:hasAssertion dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_assertion;
    np:hasProvenance dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_provenance;
    np:hasPublicationInfo dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_assertion a np:Assertion .
  
  dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_provenance a np:Provenance .
  
  dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_assertion {
  miriam-gene:57526 a ncit:C16612 .
  
  lld:C0035372 a ncit:C7057 .
  
  dgn-gda:DGN52de066aba68797be94c64ce27073a82 sio:SIO_000628 miriam-gene:57526, lld:C0035372;
    a sio:SIO_001121 .
}

dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_provenance {
  dgn-np:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_assertion dcterms:description
      "[They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with Rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the PCDH 19 gene.]. 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:22946725;
    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:NP790233.RAxfmmpd7m72fGTBIX3viBVYGQFRW4b6FqIV4VNoy_Jm0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:05+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" .
}