@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk> .
@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:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_head {
  this: np:hasAssertion dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_assertion;
    np:hasProvenance dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_provenance;
    np:hasPublicationInfo dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_assertion a np:Assertion .
  
  dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_provenance a np:Provenance .
  
  dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_assertion {
  miriam-gene:54820 a ncit:C16612 .
  
  lld:C1504404 a ncit:C7057 .
  
  dgn-gda:DGN9803865a51fbf0fa149fae630cc6c617 sio:SIO_000628 miriam-gene:54820, lld:C1504404;
    a sio:SIO_001121 .
}

dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_provenance {
  dgn-np:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_assertion dcterms:description
      "[We found that apart from a 3 mm hamartia in the temporal cortex of one MTLE case with NDE1 deletion and known hippocampal sclerosis in the other case, cortical lamination and cytoarchitecture were normal, with no differences between cases with deletion and disease controls.]. 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:22523559;
    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:NP375829.RASv-mAuq0IUZkwbrCnr0cWsjoB9RZ2aDuz4NUCG96bkk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}