@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_assertion
;
np:hasProvenance
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_provenance
;
np:hasPublicationInfo
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_assertion
a
np:Assertion
.
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_provenance
a
np:Provenance
.
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_assertion
{
miriam-gene:6531
a
ncit:C16612
.
lld:C0019337
a
ncit:C7057
.
dgn-gda:DGN98c76637bcdb959b5e3e3d2563f19804
sio:SIO_000628
miriam-gene:6531
,
lld:C0019337
;
a
sio:SIO_001121
.
}
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_provenance
{
dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_assertion
dcterms:description
"[Polymorphism of a variable number of tandem repeats (VNTR) in the 3' untranslated region of exon 15 of the SLC6A3 gene, coding for the dopamine transporter (DAT), was analysed to test whether length variation contributes to differences in the individual susceptibility to aggressive - criminal behaviour and liability to heroin dependence.]. 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:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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
<
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> , <
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
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"v2.1.0" .
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