@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE> .
@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:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_head {
  this: np:hasAssertion dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_assertion;
    np:hasProvenance dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_provenance;
    np:hasPublicationInfo dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_assertion a np:Assertion .
  
  dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_provenance a np:Provenance .
  
  dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_assertion {
  miriam-gene:1917 a ncit:C16612 .
  
  lld:C0026848 a ncit:C7057 .
  
  dgn-gda:DGNa690e5fe3d29bc73923db72ce9c6bb7a sio:SIO_000628 miriam-gene:1917, lld:C0026848;
    a sio:SIO_001121 .
}

dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_provenance {
  dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_assertion dcterms:description
      "[The significant difference in skeletal muscle mtDNA suggests that SIM or statin treatments are associated with depletion of skeletal muscle mtDNA or that patients with an underlying predisposition to SIM have lower mtDNA levels.]. 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:23312852;
    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:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:22+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" .
}