@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI> .
@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:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_head {
  this: np:hasAssertion dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_assertion;
    np:hasProvenance dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_provenance;
    np:hasPublicationInfo dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_assertion a np:Assertion .
  
  dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_provenance a np:Provenance .
  
  dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_assertion {
  miriam-gene:54407 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN803224a00658e86dec8d146dc1edafc9 sio:SIO_000628 miriam-gene:54407, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_provenance {
  dgn-np:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_assertion dcterms:description
      "[Surprisingly, immunohistochemical experiments using a polyclonal antiexcitatory amino acid transporter 2 antibody, showed a different localization of this protein in epilepsy derived tissue as compared to post mortem controls although glial markers such as glial fibrillary acidic protein and glutamine synthase showed similar patterns of staining.]. 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:10336123;
    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:NP326997.RApwnliz10FC3f_k911lLLCoMzg3d0N_kw5LzBApQPLyI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:11+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" .
}