@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg> .
@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:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_head {
  this: np:hasAssertion dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_assertion;
    np:hasProvenance dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_provenance;
    np:hasPublicationInfo dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_assertion a np:Assertion .
  
  dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_provenance a np:Provenance .
  
  dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_assertion {
  miriam-gene:6506 a ncit:C16612 .
  
  lld:C0917798 a ncit:C7057 .
  
  dgn-gda:DGN72c9a51b050ec524d4ad45ece68e373b sio:SIO_000628 miriam-gene:6506, lld:C0917798;
    a sio:SIO_001121 .
}

dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_provenance {
  dgn-np:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_assertion dcterms:description
      "[We will also describe the finding of a novel polymorphism in the EAAT2 promoter region which could be responsible for differences in both gene function and regulation under pathological conditions such as cerebral ischemia, and which might well account for the failure of glutamate antagonists in the clinical practice.]. 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:16651809;
    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:NP239154.RAUtXgedVvTBmn8xcOUK4vWRWwbDEEOuuweEMXVYUjhBg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
}