@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0> .
@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:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_head {
   this: np:hasAssertion dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_assertion ;
    np:hasProvenance dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_provenance ;
    np:hasPublicationInfo dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_assertion a np:Assertion .
  dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_provenance a np:Provenance .
  dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_assertion {
   miriam-gene:4566 a ncit:C16612 .
  lld:C0025362 a ncit:C7057 .
  dgn-gda:DGN2b758813030ae57fb741be0811c413a9 sio:SIO_000628 miriam-gene:4566 , lld:C0025362 ;
    a sio:SIO_001121 .
}
dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_provenance {
   dgn-np:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_assertion dcterms:description "[Patients showed heterogeneous phenotypes including Leigh disease in four, MELAS in six, unclassified mitochondrial myopathy in 10, cardiomyopathy in five, MERRF in one, pure lactic acidosis in six, and others in 12 including facio-scaplo-femoral muscular dystrophy (FSFD), familial cerebellar ataxia, recurrent Reye syndrome, cerebral palsy with mental retardation.]. 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:16337222 ;
    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:NP274851.RAbY4529QJVCwLw66ZnPtEWsBgHDk7kbeP77AAZhGY4H0130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:34+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" .
}