@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_head {
  this: np:hasAssertion dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_assertion;
    np:hasProvenance dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_provenance;
    np:hasPublicationInfo dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_assertion a np:Assertion .
  
  dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_provenance a np:Provenance .
  
  dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_assertion {
  miriam-gene:5428 a ncit:C16612 .
  
  lld:C1843920 a ncit:C7057 .
  
  dgn-gda:DGNef49c61b9722848411be7283b43122e9 sio:SIO_000628 miriam-gene:5428, lld:C1843920;
    a sio:SIO_001121 .
}

dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_provenance {
  dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_assertion dcterms:description
      "[Most recently described mitochondrial myopathies are due to defects in nuclear DNA, including coenzyme Q10 deficiency, and mutations in genes that control mitochondrial DNA (mtDNA) abundance and structure such as POLG and TK2.]. 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:16155436;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:37+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}