@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA> .
@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:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_head {
  this: np:hasAssertion dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_assertion;
    np:hasProvenance dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_provenance;
    np:hasPublicationInfo dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_assertion a np:Assertion .
  
  dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_provenance a np:Provenance .
  
  dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_assertion {
  miriam-gene:23583 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGN376dcbab8644b23812575141981ecbee sio:SIO_000628 miriam-gene:23583, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_provenance {
  dgn-np:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_assertion dcterms:description
      "[Based on the detailed examination using MRI and FDG-PET for two of the patients, the authors hypothesize hyperexcitability caused by the decreased inhibitory functions, larger number of synchronously activated neurons, or the elongation of neuronal firing in the pathological temporal cortex in ADLTE.]. 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:19793676;
    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:NP568869.RAZXrTfyI7uZYtezLaqM10d5E86nnYwBwsT5t0b5FPBhA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:43+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}