@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA
> .
@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:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_head
{
this:
np:hasAssertion
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_assertion
;
np:hasProvenance
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_provenance
;
np:hasPublicationInfo
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_assertion
a
np:Assertion
.
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_provenance
a
np:Provenance
.
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C0086132
a
ncit:C7057
.
dgn-gda:DGN2cd022764418edfe8fa8d0416f12ede9
sio:SIO_000628
miriam-gene:1557
,
lld:C0086132
;
a
sio:SIO_001121
.
}
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_provenance
{
dgn-np:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_assertion
dcterms:description
"[The Sequenced Treatment Alternatives to Relieve Depression sample was used to examine the relationship between variations in the CYP2C19 and CYP2D6 genes and remission of depressive symptoms and tolerance to treatment with citalopram.]. 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:21192344
;
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:NP760986.RAfNeXewTFSD7Lh-MDQUD_3VgrvSfSzhKRvCb3lnkmcbA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}