@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP838034.RAk_B3Co-LuyRHtjIc6ExKvMJHHYJ4WZurR1_RbE6XgAo
> .
@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/v4.0.0/void/
> .
dgn-np:NP838034.RAk_B3Co-LuyRHtjIc6ExKvMJHHYJ4WZurR1_RbE6XgAo130_head
{
this:
np:hasAssertion
dgn-np:NP838034.RAk_B3Co-LuyRHtjIc6ExKvMJHHYJ4WZurR1_RbE6XgAo130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP838034.RAk_B3Co-LuyRHtjIc6ExKvMJHHYJ4WZurR1_RbE6XgAo130_provenance
a
np:Provenance
.
dgn-np:NP838034.RAk_B3Co-LuyRHtjIc6ExKvMJHHYJ4WZurR1_RbE6XgAo130_publicationInfo
a
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.
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{
miriam-gene:2784
a
ncit:C16612
.
lld:C1269683
a
ncit:C7057
.
dgn-gda:DGN610f6ba83e0372f3708842c1b7c814cc
sio:SIO_000628
miriam-gene:2784
,
lld:C1269683
;
a
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.
}
dgn-np:NP838034.RAk_B3Co-LuyRHtjIc6ExKvMJHHYJ4WZurR1_RbE6XgAo130_provenance
{
dgn-np:NP838034.RAk_B3Co-LuyRHtjIc6ExKvMJHHYJ4WZurR1_RbE6XgAo130_assertion
dcterms:description
"[We here report analysis of data from GENDEP, a part-randomized pharmacogenomic trial, on the outcome of 811 subjects with major depression undergoing treatment with either escitalopram or nortriptyline in which the C825T SNP and three further SNPs in GNB3 were genotyped.]. 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:20826553
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP838034.RAk_B3Co-LuyRHtjIc6ExKvMJHHYJ4WZurR1_RbE6XgAo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:04+02:00"^^
xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
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> ;
pav:createdBy
<
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> ;
pav:version
"v4.0.0.0" .
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"v4.0.0" .
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