@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4> .
@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:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_head {
  this: np:hasAssertion dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_assertion;
    np:hasProvenance dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_provenance;
    np:hasPublicationInfo dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_assertion a np:Assertion .
  
  dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_provenance a np:Provenance .
  
  dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_assertion {
  miriam-gene:54790 a ncit:C16612 .
  
  lld:C0162674 a ncit:C7057 .
  
  dgn-gda:DGN5ebe33d679ccc3bb901db65760ffa3b4 sio:SIO_000628 miriam-gene:54790, lld:C0162674;
    a sio:SIO_001121 .
}

dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_provenance {
  dgn-np:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_assertion dcterms:description
      "[Future studies on MNGIE and adPEO pathogenesis, and identification of additional gene defects in adPEO and MDS will provide further understanding about the mammalian mtDNA maintenance and the crosstalk between the nuclear and mitochondrial genomes.]. 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:11579425;
    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:NP876660.RARV2vZRoWGTt6CeG0hFuoqwQuIvmh6Y0xf6UYm1lNwL4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:55+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;
    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" .
}