@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ
> .
@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:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_head
{
this:
np:hasAssertion
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_assertion
;
np:hasProvenance
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_assertion
a
np:Assertion
.
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_provenance
a
np:Provenance
.
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C1842981
a
ncit:C7057
.
dgn-gda:DGN430fcd3f47715ef59f23ac402fdccf73
sio:SIO_000628
miriam-gene:6532
,
lld:C1842981
;
a
sio:SIO_001121
.
}
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_provenance
{
dgn-np:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_assertion
dcterms:description
"[A functional polymorphism in the promoter region of the human serotonin transporter gene (SLC6A4) has been associated with several dimensions of neuroticism and psychopathology, especially anxiety traits, but the predictive value of this genotype against these complex behaviors has been inconsistent.]. 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:12130784
;
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:NP271364.RABjpK9xM_GtPuwHemHiThidxscJJWULgjzgtRQKKU_qQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:31+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" .
}