@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc> .
@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:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_head {
  this: np:hasAssertion dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_assertion;
    np:hasProvenance dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_provenance;
    np:hasPublicationInfo dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_assertion a np:Assertion .
  
  dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_provenance a np:Provenance .
  
  dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_assertion {
  miriam-gene:4536 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN482a19ad32572141b85b169b4e3a7517 sio:SIO_000628 miriam-gene:4536, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_provenance {
  dgn-np:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_assertion dcterms:description
      "[A specific mitochondrial DNA mutation at position 5460 in the ND2 gene of the human mitochondrial genome was recently reported to exist in 10 of 19 patients with Alzheimer's disease, implying an association between this mtDNA mutation and the occurrence of the disease.]. 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:1352971;
    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:NP637878.RAS93KcG7o5GncNEp06aLjwporvE4sZ8ZQ-FpoPigdNnc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:24+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" .
}