@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI
> .
@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:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_head
{
this:
np:hasAssertion
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_assertion
;
np:hasProvenance
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_provenance
;
np:hasPublicationInfo
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_assertion
a
np:Assertion
.
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_provenance
a
np:Provenance
.
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_assertion
{
miriam-gene:2644
a
ncit:C16612
.
lld:C0041696
a
ncit:C7057
.
dgn-gda:DGN780889913730e70a9dab82c6e4ee045a
sio:SIO_000628
miriam-gene:2644
,
lld:C0041696
;
a
sio:SIO_001121
.
}
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_provenance
{
dgn-np:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_assertion
dcterms:description
"[Given the pivotal role of the serotonergic system in mood disorders and selective serotonin reuptake inhibitors (SSRIs) antidepressant function, we tested the hypothesis that GFRP gene (GCHFR) variants would modify response to antidepressants in subjects with major depression.]. 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:20351752
;
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:NP766587.RAL9VGyQjrM87HgDYLkxMA8WaKFeFT19w_EATHoPK8nUI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}