@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk> .
@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:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_head {
  this: np:hasAssertion dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_assertion;
    np:hasProvenance dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_provenance;
    np:hasPublicationInfo dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_assertion a np:Assertion .
  
  dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_provenance a np:Provenance .
  
  dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_assertion {
  miriam-gene:8912 a ncit:C16612 .
  
  lld:C0014553 a ncit:C7057 .
  
  dgn-gda:DGNeaa87d3717e58c2dafb5cb3f38ef474a sio:SIO_000628 miriam-gene:8912, lld:C0014553;
    a sio:SIO_001121 .
}

dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_provenance {
  dgn-np:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_assertion dcterms:description
      "[CACNA1H is a human gene encoding Ca(v)3.2 low-voltage-activated, T-type calcium channels associated with bursting behavior in neurons and has been linked to more than 30 mutations apparently predisposing to childhood absence epilepsy (CAE) and other idiopathic generalized epilepsies (IGEs).]. 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:16565161;
    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:NP208686.RA9yn7zhSglKEQuL4xnFNrynLXezi2aC_jLukNqsyjbCk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:55+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" .
}