@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs> .
@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:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_head {
  this: np:hasAssertion dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_assertion;
    np:hasProvenance dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_provenance;
    np:hasPublicationInfo dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_assertion a np:Assertion .
  
  dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_provenance a np:Provenance .
  
  dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_assertion {
  miriam-gene:121278 a ncit:C16612 .
  
  lld:C0525045 a ncit:C7057 .
  
  dgn-gda:DGN1787b319778f067d6c0dc7ae86d3a79a sio:SIO_000628 miriam-gene:121278, lld:C0525045;
    a sio:SIO_001121 .
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dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_provenance {
  dgn-np:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_assertion dcterms:description
      "[The main conclusions of the review are: i) there is an association between TPH2 and genetically defined behavioral variations, ii) the haplotypes, including some human TPH2 gene SNPs, can predict the risk of affective disorders and the sensitivity to antidepressant therapeutics, iii) mutations decreasing TPH2 activity produce negative effects on behavior and, possibly, on survival, iv) the effect of dietary tryptophan manipulations on human mood and behavior is modest compared with that of inhibitors of 5-HT transporter and monoamine oxidase.]. 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:20874521;
    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:NP400696.RA3RfoP6YIwU2uuBEHKA7tgoe94BDryKFf491QvYn4IPs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:58+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" .
}