@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik> .
@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:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_head {
  this: np:hasAssertion dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_assertion;
    np:hasProvenance dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_provenance;
    np:hasPublicationInfo dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_assertion a np:Assertion .
  
  dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_provenance a np:Provenance .
  
  dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_assertion {
  miriam-gene:124935 a ncit:C16612 .
  
  lld:C2675211 a ncit:C7057 .
  
  dgn-gda:DGNaee7e30ba296350fb01fc65e1429a4f4 sio:SIO_000628 miriam-gene:124935, lld:C2675211;
    a sio:SIO_001121 .
}

dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_provenance {
  dgn-np:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_assertion dcterms:description
      "[Episodic ataxia type 6 represents the first human disease found to be associated with altered function of excitatory amino acid transporter anion channels and illustrates possible physiological and pathophysiological impacts of this functional mode of this class of glutamate transporters.]. 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:23107647;
    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:NP844459.RAjwXJQwWeJtYoEJJWpPvNIzmnZpp7wr4AAB_DSL59zik130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:36+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" .
}