@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE> .
@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:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_head {
  this: np:hasAssertion dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_assertion;
    np:hasProvenance dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_provenance;
    np:hasPublicationInfo dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_assertion a np:Assertion .
  
  dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_provenance a np:Provenance .
  
  dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_assertion {
  miriam-gene:1371 a ncit:C16612 .
  
  lld:C0268237 a ncit:C7057 .
  
  dgn-gda:DGN26419dcd64159c5f0fd49a2a1a8c18ce sio:SIO_000628 miriam-gene:1371, lld:C0268237;
    a sio:SIO_001121 .
}

dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_provenance {
  dgn-np:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_assertion dcterms:description
      "[Our report of two patients with isolated COX deficiency and new mutations in COX subunit genes may help to draw more attention to this type of mtDNA defects and provide new aspects for counselling affected families.]. 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:16288875;
    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:NP230070.RAfp18YST12cGDL4nTHMhKZN8FrYyA9dubcs21LW7rGLE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}