@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c> .
@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:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_head {
  this: np:hasAssertion dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_assertion;
    np:hasProvenance dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_provenance;
    np:hasPublicationInfo dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_assertion a np:Assertion .
  
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  dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_assertion {
  miriam-gene:170302 a ncit:C16612 .
  
  lld:C0266463 a ncit:C7057 .
  
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dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_provenance {
  dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_assertion dcterms:description
      "[In this review we report on our experience and review the existing literature on the genotype and phenotype heterogeneity associated with ARX abnormalities in humans ranging from severe neuronal migration defects (e.g., lissencephaly), to mild forms of X-linked mental retardation without apparent brain abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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 .
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dgn-np:NP789043.RAzojTC6sPoy2wqt1JxpahBshgOHTMD4gcTFEQ1dTiG0c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:01+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;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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