@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg> .
@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:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_head {
  this: np:hasAssertion dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_assertion;
    np:hasProvenance dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_provenance;
    np:hasPublicationInfo dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_assertion a np:Assertion .
  
  dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_provenance a np:Provenance .
  
  dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_assertion {
  miriam-gene:6531 a ncit:C16612 .
  
  lld:C1457883 a ncit:C7057 .
  
  dgn-gda:DGN8ff52aa0041a616ae15a0a90aa5f027a sio:SIO_000628 miriam-gene:6531, lld:C1457883;
    a sio:SIO_001121 .
}

dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_provenance {
  dgn-np:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_assertion dcterms:description
      "[The regression analysis of BDHI subscales, performed to provide an estimate of the magnitude of any potential effect on the risk of aggressiveness associated with the variants in DAT VNTR, showed that the presence of the 9 - 9 genotype significantly increases the risk of irritability and direct aggressiveness more than six and 10 times with respect to the 9 - 10 genotype.]. 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:16109590;
    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:NP704750.RApMs167mqoz2vRv2R8qD_TxrKycF2ra2f4ukdm0BbKGg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}