@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs> .
@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:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_head {
   this: np:hasAssertion dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_assertion ;
    np:hasProvenance dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_provenance ;
    np:hasPublicationInfo dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_assertion a np:Assertion .
  dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_provenance a np:Provenance .
  dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_assertion {
   miriam-gene:56652 a ncit:C16612 .
  lld:C0751651 a ncit:C7057 .
  dgn-gda:DGN12b6984f5f22e544049a6685639b1843 sio:SIO_000628 miriam-gene:56652 , lld:C0751651 ;
    a sio:SIO_001121 .
}
dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_provenance {
   dgn-np:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_assertion dcterms:description "[The aim of this study was to evaluate the exercise capacity and lactate kinetics related to exercise in subjects with two genetically characterized mitochondrial disorders (multiple mitochondrial DNA deletions with PEO, MELAS) compared with lactate kinetics in subjects with metabolic myopathy (McArdle's disease) and in the healthy controls.]. 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:15056184 ;
    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:NP607796.RAfW2FWMamNVsvml9vkji__7VVL9_mkLaCcUYm_wfCUqs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:05+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" .
}