@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI
> .
@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:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_head
{
this:
np:hasAssertion
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_assertion
;
np:hasProvenance
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_provenance
;
np:hasPublicationInfo
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_assertion
a
np:Assertion
.
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_provenance
a
np:Provenance
.
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_assertion
{
miriam-gene:121278
a
ncit:C16612
.
lld:C0041696
a
ncit:C7057
.
dgn-gda:DGNb8c98c7fc812283cae8c864fa7805d34
sio:SIO_000628
miriam-gene:121278
,
lld:C0041696
;
a
sio:SIO_001121
.
}
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_provenance
{
dgn-np:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_assertion
dcterms:description
"[The mechanisms underlying these changes are uncertain, but increased TPH2 expression and serotonin turnover could result from genetic influences, adverse early life experiences, or acute stressful life events, all of which can alter serotonergic neurotransmission and have been implicated in determining vulnerability to 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:19120094
;
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:NP681280.RA5kwmLiaaRg9elb58zqkUo1jP2amifKUBtDTN_z0hFBI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:51+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" .
}