@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc> .
@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:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_head {
  this: np:hasAssertion dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_assertion;
    np:hasProvenance dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_provenance;
    np:hasPublicationInfo dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_assertion a np:Assertion .
  
  dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_provenance a np:Provenance .
  
  dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_assertion {
  miriam-gene:4128 a ncit:C16612 .
  
  lld:C0525045 a ncit:C7057 .
  
  dgn-gda:DGN061d2898fc3cf37295ba0a1a0eddcbe4 sio:SIO_000628 miriam-gene:4128, lld:C0525045;
    a sio:SIO_001121 .
}

dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_provenance {
  dgn-np:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_assertion dcterms:description
      "[In order to determine the possible role of the MAO region in susceptibility to affective disorders in an independent sample, we have genotyped 83 probands of bipolar affective disorder families, 56 sets of parents of bipolar probands, and 84 normal controls for intronic simple sequence repeat polymorphisms of the MAO-A and MAO-B genes.]. 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:9342194;
    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:NP497509.RAcyBirAYdTSsstqTi1xJC1sC8iU75-7oeZdRD-5JoHxc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+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" .
}