@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE
> .
@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:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_head
{
this:
np:hasAssertion
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_assertion
;
np:hasProvenance
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_provenance
;
np:hasPublicationInfo
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_assertion
a
np:Assertion
.
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_provenance
a
np:Provenance
.
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0038586
a
ncit:C7057
.
dgn-gda:DGN3be625c2a8d2126c203eaeac811dc17c
sio:SIO_000628
miriam-gene:1312
,
lld:C0038586
;
a
sio:SIO_001121
.
}
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_provenance
{
dgn-np:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_assertion
dcterms:description
"[One hundred seven methadone maintenance treatment patients, 36 having an ADHD diagnosis, 176 adult patients with ADHD without SUDs, and 500 healthy controls were genotyped for variants in the DRD4 (exon 3 VNTR), DRD5 (upstream VNTR), HTR1B (rs6296), DBH (rs2519152), COMT (rs4680; Val158Met), and OPRM1 (rs1799971; 118A>G) genes.]. 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:22841130
;
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:NP163851.RAVpDHM5A-cRT-x-dJd6Sp5WCipV9J0yh7M5HeKY9NvjE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}