@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE> .
@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:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_head {
  this: np:hasAssertion dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_assertion;
    np:hasProvenance dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_provenance;
    np:hasPublicationInfo dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_assertion a np:Assertion .
  
  dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_provenance a np:Provenance .
  
  dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_assertion {
  miriam-gene:1890 a ncit:C16612 .
  
  lld:C0751651 a ncit:C7057 .
  
  dgn-gda:DGN3cbe32b531a96710ffc869e1da1efb38 sio:SIO_000628 miriam-gene:1890, lld:C0751651;
    a sio:SIO_001121 .
}

dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_provenance {
  dgn-np:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_assertion dcterms:description
      "[This review focuses on our current knowledge of genetic defects of mtDNA replication (POLG, POLG2, C10orf2) and nucleotide metabolism (TYMP, TK2, DGOUK, and RRM2B) that cause instability of mtDNA and mitochondrial disease.]. 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:22176657;
    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:NP704566.RA7inYBcUhsewTdxQ_H4fyT_Sotvl67oCbEd-IsltrFdE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}