@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg> .
@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:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_head {
  this: np:hasAssertion dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_assertion ;
    np:hasProvenance dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_provenance ;
    np:hasPublicationInfo dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_assertion a np:Assertion .
  dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_provenance a np:Provenance .
  dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_assertion {
  miriam-gene:9377 a ncit:C16612 .
  lld:C0162671 a ncit:C7057 .
  dgn-gda:DGN67828197d09423dec2c0eaa4eb2035d1 sio:SIO_000628 miriam-gene:9377 , lld:C0162671 ;
    a sio:SIO_001121 .
}
dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_provenance {
  dgn-np:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_assertion dcterms:description "[We also describe systemic manifestations of MELAS-associated mutations, including cardiac, renal, endocrine, gastrointestinal, and endothelial abnormalities and pathology, as well as the hypothetical role of derangements to COX enzymatic function in driving the unique pathology and clinical manifestations of MELAS.]. 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:18990125 ;
    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:NP243022.RAzi0MSCqGotHDgG4pLHFTYsXMYN4Ty7bYF8S9xkJegwg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:16+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" .
}