@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc> .
@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:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_head {
  this: np:hasAssertion dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_assertion;
    np:hasProvenance dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_provenance;
    np:hasPublicationInfo dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_assertion a np:Assertion .
  
  dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_provenance a np:Provenance .
  
  dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_assertion {
  miriam-gene:4541 a ncit:C16612 .
  
  lld:C0917796 a ncit:C7057 .
  
  dgn-gda:DGN7df3eb6957e68ecdc2af0ebf2d730aa3 sio:SIO_000628 miriam-gene:4541, lld:C0917796;
    a sio:SIO_001121 .
}

dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_provenance {
  dgn-np:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_assertion dcterms:description
      "[Mitochondrial DNA mutations at nucleotide position (np) 3460 in the ND1 gene, np 11778 in the ND4 gene, and np 14484 in the ND6 gene are commonly considered to be associated with the clinical features of LHON and account for the majority of LHON cases.]. 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:12271374;
    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:NP448635.RAb3bhFKy_SEXJV_2CtoSYopAsb5XHxBQNyDEdPkBwfDc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:27+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" .
}