@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0> .
@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:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_head {
  this: np:hasAssertion dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_assertion;
    np:hasProvenance dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_provenance;
    np:hasPublicationInfo dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_assertion a np:Assertion .
  
  dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_provenance a np:Provenance .
  
  dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_assertion {
  miriam-gene:9377 a ncit:C16612 .
  
  lld:C0268237 a ncit:C7057 .
  
  dgn-gda:DGN45fa0dfecde497cb01ada072b5ea5212 sio:SIO_000628 miriam-gene:9377, lld:C0268237;
    a sio:SIO_001121 .
}

dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_provenance {
  dgn-np:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_assertion dcterms:description
      "[Consequently, cytochrome oxidase (COX) deficiency was found in all these (LS(COX)) cell lines and, thus, the main mitochondrial mechanism of generation of the electrochemical proton gradient on the mitochondrial membrane was naturally depressed.]. 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:11341780;
    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:NP273563.RASp7XXmbs7L_1KflKpxSNN_8232pHTu3c90ozuX-Rrp0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:34+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" .
}