@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs> .
@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:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_head {
  this: np:hasAssertion dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_assertion;
    np:hasProvenance dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_provenance;
    np:hasPublicationInfo dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_assertion a np:Assertion .
  
  dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_provenance a np:Provenance .
  
  dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_assertion {
  miriam-gene:4128 a ncit:C16612 .
  
  lld:C0525045 a ncit:C7057 .
  
  dgn-gda:DGN56e1315b1638d90154d802e3f16adcc7 sio:SIO_000628 miriam-gene:4128, lld:C0525045;
    a sio:SIO_001122 .
}

dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_provenance {
  dgn-np:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_assertion dcterms:description
      "[To ascertain whether mood disorders, including bipolar and unipolar, are genetically associated with the monoamine oxidase A (MAOA) or monoamine oxidase B (MAOB) gene in the Chinese population, 132 cases of mood disorder and 88 normal controls were genotyped for the MAOA(CA)n, MAOB(GT)n, and MAOB(TG)n loci by the method of amplification fragment length polymorphism.]. 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:10686545;
    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:NP54970.RAcxabmSLO74nO_nitpr-Ewb8gDxoQfOtciaeurP_lAqs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}