@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI
> .
@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:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_head
{
this:
np:hasAssertion
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_assertion
;
np:hasProvenance
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_provenance
;
np:hasPublicationInfo
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_assertion
a
np:Assertion
.
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_provenance
a
np:Provenance
.
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_assertion
{
miriam-gene:627
a
ncit:C16612
.
lld:C0031212
a
ncit:C7057
.
dgn-gda:DGN37ae63039a7568e98a6dee1be24c5e51
sio:SIO_000628
miriam-gene:627
,
lld:C0031212
;
a
sio:SIO_001121
.
}
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_provenance
{
dgn-np:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_assertion
dcterms:description
"[The low activity variants of the 5-HTT-linked polymorphic region in the serotonin transporter gene and the Met-allele of a single nucleotide polymorphism (Val66Met) in the gene encoding brain derived neurotrophic factor were independently associated with the presence of stressful life events prior to onset of depression, also when corrected for the effect of age, gender, marital status, personality disorder, neuroticism, and severity of depressive symptoms at the time of interview.]. 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:19339052
;
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:NP557786.RAODlyPILZVrsLTNTUlC5yjlM3tlncmNzUJb8qc0ZfVzI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}