@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0> .
@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:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_head {
  this: np:hasAssertion dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_assertion;
    np:hasProvenance dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_provenance;
    np:hasPublicationInfo dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_assertion a np:Assertion .
  
  dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_provenance a np:Provenance .
  
  dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_assertion {
  miriam-gene:9927 a ncit:C16612 .
  
  lld:C0338508 a ncit:C7057 .
  
  dgn-gda:DGNbea4c08a89d58181f67dd81ad7519f27 sio:SIO_000628 miriam-gene:9927, lld:C0338508;
    a sio:SIO_001121 .
}

dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_provenance {
  dgn-np:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_assertion dcterms:description
      "[The clinical relevance of maintaining a finely tuned balance between mitochondrial fusion and fission processes is underscored by the fact that the pathogenesis of certain hereditary neurodegenerative disorders such as autosomal dominant optic atrophy (ADOA) and Charcot-Marie-Tooth neuropathy type 2A (CMT2A) can now be linked to mutations in genes encoding mediators of mitochondrial fusion.]. 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:16468021;
    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:NP685865.RAP89HepcPmfhApTZSNNEAMvRq1PverPZQhaxL2m66hx0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:57+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" .
}