@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo> .
@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#> .
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   this: np:hasAssertion dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_assertion ;
    np:hasProvenance dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_provenance ;
    np:hasPublicationInfo dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_provenance a np:Provenance .
  dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_assertion {
   miriam-gene:4128 a ncit:C16612 .
  lld:C0740858 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_provenance {
   dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_assertion dcterms:description "[We have therefore typed polymorphisms at the serotonin transporter, dopamine receptor, tryptophan hydroxylase, tyrosine hydoxylase, and monoamine oxidase A (MAOA) loci in 139 unipolar and 131 bipolar patients and investigated associations with gender, number of episodes, age of onset, history of psychotic symptoms, history of suicidal behavior, and history of substance abuse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP757739.RAGUpnUehe96V4zVrKIToQHXQ6H7pEq-j_0MxO_0XQXHo130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:39+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> ;
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}