@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0> .
@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:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_head {
  this: np:hasAssertion dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_assertion ;
    np:hasProvenance dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_provenance ;
    np:hasPublicationInfo dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_assertion a np:Assertion .
  dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_provenance a np:Provenance .
  dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_assertion {
  miriam-gene:7166 a ncit:C16612 .
  lld:C0001807 a ncit:C7057 .
  dgn-gda:DGN8781b557a805a7920982393be3c6a138 sio:SIO_000628 miriam-gene:7166 , lld:C0001807 ;
    a sio:SIO_001122 .
}
dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_provenance {
  dgn-np:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_assertion dcterms:description "[Finally, an association study with 58 volunteers revealed that the A779C TPH polymorphism significantly relates to AH, with the highest aggression levels for the genotype AA and the lowest aggression levels for the genotype CC, but not to NH. Results are discussed with respect to inconsistent findings in the literature, which may be explained by this distinction of types of aggression.]. 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:15727508 ;
    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:NP58784.RAE3zsx-8nIt4p35HiGkN_cgG-xd3BzGZB1GquLSRXqW0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}