@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk> .
@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:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_head {
  this: np:hasAssertion dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_assertion;
    np:hasProvenance dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_provenance;
    np:hasPublicationInfo dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_assertion a np:Assertion .
  
  dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_provenance a np:Provenance .
  
  dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_assertion {
  miriam-gene:7217 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
  dgn-gda:DGNc75cdeb42a5084704dcd63177f1f9cb0 sio:SIO_000628 miriam-gene:7217, lld:C0005586;
    a sio:SIO_001122 .
}

dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_provenance {
  dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_assertion dcterms:description
      "[The 5178C/10398A haplotype in mtDNA may be a risk factor of bipolar disorder (odds ratio, 2.4). Pathophysiological significance of rare mtDNA mutations needs to be verified in the future. This finding may imply the pathophysiological significance of mtDNA in bipolar disorder.]. 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:11223103;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}