@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0> .
@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/v3.0.0/void/> .
dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_head {
  this: np:hasAssertion dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_assertion ;
    np:hasProvenance dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_provenance ;
    np:hasPublicationInfo dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_assertion a np:Assertion .
  dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_provenance a np:Provenance .
  dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_assertion {
  miriam-gene:6531 a ncit:C16612 .
  lld:C0004936 a ncit:C7057 .
  dgn-gda:DGNa5fc2a9da019080a0d97691f21a038da sio:SIO_000628 miriam-gene:6531 , lld:C0004936 ;
    a sio:SIO_001121 .
}
dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_provenance {
  dgn-np:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_assertion dcterms:description "[We have demonstrated in both the human serotonin transporter gene (5HTT) and the dopamine transporter gene (DAT1) that specific polymorphic variants termed Variable Number Tandem Repeats (VNTRs), which correlate with predisposition to a number of neurological and psychiatric disorders, act as transcriptional regulatory domains.]. 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:17960477 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP698235.RABgs_pPtu1DL8jhTZVV656-2I2QX5y2JFlOUY5VCtoI0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:41+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}