@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso> .
@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:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_head {
  this: np:hasAssertion dgn-np:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_assertion;
    np:hasProvenance dgn-np:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_provenance;
    np:hasPublicationInfo dgn-np:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_provenance a np:Provenance .
  
  dgn-np:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_assertion {
  miriam-gene:55669 a ncit:C16612 .
  
  lld:C0338508 a ncit:C7057 .
  
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dgn-np:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_provenance {
  dgn-np:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_assertion dcterms:description
      "[We found increased expression of the mitochondrial fission genes Drp1 and Fis1 (fission 1) and decreased expression of the mitochondrial fusion genes Mfn1 (mitofusin 1), Mfn2 (mitofusin 2), Opa1 (optic atrophy 1) and Tomm40.]. 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:21459773;
    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:NP590492.RAQK_QG9rqYpVBILGqE2lt0ek3OVRYaUYKzulfTL4BLso130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:55+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;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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