@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8> .
@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:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_head {
  this: np:hasAssertion dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_assertion;
    np:hasProvenance dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_provenance;
    np:hasPublicationInfo dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_assertion a np:Assertion .
  
  dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_provenance a np:Provenance .
  
  dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_assertion {
  miriam-gene:4128 a ncit:C16612 .
  
  lld:C0038663 a ncit:C7057 .
  
  dgn-gda:DGN2181c12f325d23161bdbc8a07831a66e sio:SIO_000628 miriam-gene:4128, lld:C0038663;
    a sio:SIO_001121 .
}

dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_provenance {
  dgn-np:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_assertion dcterms:description
      "[As both genes are involved in degrading noradreanline, we also tested the hypothesis of epistasis between MAOA polymorphisms and Val158Met, however, no additive effect was found in conferring risk for suicide attempt.]. 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:15936529;
    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:NP376779.RAaJ9isYz_FQslLn6olpapdJvT5RkZjpB8jawTllxMns8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}