@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM> .
@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:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_head {
  this: np:hasAssertion dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_assertion;
    np:hasProvenance dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_provenance;
    np:hasPublicationInfo dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_assertion a np:Assertion .
  
  dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_provenance a np:Provenance .
  
  dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_assertion {
  miriam-gene:1760 a ncit:C16612 .
  
  lld:C0231528 a ncit:C7057 .
  
  dgn-gda:DGNbb7bb75980316fea9a94f5b58c5c4bbe sio:SIO_000628 miriam-gene:1760, lld:C0231528;
    a sio:SIO_001121 .
}

dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_provenance {
  dgn-np:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_assertion dcterms:description
      "[The candidate genes COQ2, ATP2B1, and DMPK, representing pathways involved in myocellular energy transfer, calcium homeostasis, and myotonic dystonia, respectively, were validated as markers for the common myalgia observed in patients receiving statin therapy.]. 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:21868014;
    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:NP284670.RAAwOXV4dQNGPORwKnu0pTWWwVp4bXvXzoHrp71AAaPlM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:40+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" .
}