@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc
> .
@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:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_head
{
this:
np:hasAssertion
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_assertion
;
np:hasProvenance
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_provenance
;
np:hasPublicationInfo
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_assertion
a
np:Assertion
.
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_provenance
a
np:Provenance
.
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_assertion
{
miriam-gene:2004
a
ncit:C16612
.
lld:C1263846
a
ncit:C7057
.
dgn-gda:DGNebd2ae4074f1b6a6c60d5a04295f4407
sio:SIO_000628
miriam-gene:2004
,
lld:C1263846
;
a
sio:SIO_001121
.
}
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_provenance
{
dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_assertion
dcterms:description
"[The norepinephrine transporter (NET, SLC6A2) represents an important candidate gene for contribution to ADHD because it regulates catecholamine extracellular and tissue concentrations and contributes to executive functions disrupted in ADHD, and NET is a target for most effective ADHD therapeutics.]. 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:19698724
;
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:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}