@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs> .
@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:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_head {
  this: np:hasAssertion dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_assertion;
    np:hasProvenance dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_provenance;
    np:hasPublicationInfo dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_assertion a np:Assertion .
  
  dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_provenance a np:Provenance .
  
  dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_assertion {
  miriam-gene:170302 a ncit:C16612 .
  
  lld:C0266463 a ncit:C7057 .
  
  dgn-gda:DGN70995ac6728b001562ba7aaf9f1c0935 sio:SIO_000628 miriam-gene:170302, lld:C0266463;
    a sio:SIO_001121 .
}

dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_provenance {
  dgn-np:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_assertion dcterms:description
      "[In summary, analysis of the ARX gene should not only be considered in male patients with typical features of XLAG but also in those presenting with early onset epilepsy, ACC, and abnormal genitalia without obvious neuroradiological features of lissencephaly.]. 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:15248097;
    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:NP683690.RAkArhn7vBlv0UvESeaTKBHYUVNKIkDK8FZBHrCxbbAOs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}