@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_head {
  this: np:hasAssertion dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_assertion;
    np:hasProvenance dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_provenance;
    np:hasPublicationInfo dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_assertion a np:Assertion .
  
  dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_provenance a np:Provenance .
  
  dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_assertion {
  miriam-gene:4538 a ncit:C16612 .
  
  lld:C0029132 a ncit:C7057 .
  
  dgn-gda:DGNc93e894974516cd48e54de985e00b88d sio:SIO_000628 miriam-gene:4538, lld:C0029132;
    a sio:SIO_001121 .
}

dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_provenance {
  dgn-np:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_assertion dcterms:description
      "[The occurrence of optic neuropathy in patients with MS-like disorders who carry one of the pathogenetically significant LHON mutations as well as the higher incidence of maternal transmission in familial cases of MS support the hypothesis that mitochondrial genes may be implicated in susceptibility to MS. We sequenced the entire mtDNA of six children with MS who developed optic neuritis as early and prominent visual involvement.]. 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:9762692;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP576584.RAtRh68-augh3-0DF8zfgM3UnF26RxapefU_JiThpmkSM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:23+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}