@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_head {
  this: np:hasAssertion dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_assertion ;
    np:hasProvenance dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_provenance ;
    np:hasPublicationInfo dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_assertion a np:Assertion .
  dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_provenance a np:Provenance .
  dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_assertion {
  miriam-gene:6532 a ncit:C16612 .
  lld:C1842981 a ncit:C7057 .
  dgn-gda:DGNde884578534de91da8db000333623b5e sio:SIO_000628 miriam-gene:6532 , lld:C1842981 ;
    a sio:SIO_001121 .
}
dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_provenance {
  dgn-np:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_assertion dcterms:description "[The strongest effects occurred in those infants with the s/s 5-HTTLPR polymorphism who also were lacking long D4DR alleles which in some studies has been linked to adult novelty seeking.1,6 These infants showed most negative emotionality and most distress to daily situations, temperament traits that are perhaps the underpinning of adult neuroticism.]. 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:10483054 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP262791.RACJPqj_igz-XXXzko5OXQEi61rjRuPQafERgFEVBVdKs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:45+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}