@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0
> .
@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:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_head
{
this:
np:hasAssertion
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_assertion
;
np:hasProvenance
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_provenance
;
np:hasPublicationInfo
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_assertion
a
np:Assertion
.
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_provenance
a
np:Provenance
.
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_assertion
{
miriam-gene:3350
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGN34eb0abe09f508da51fe23d8ca904adf
sio:SIO_000628
miriam-gene:3350
,
lld:C0011570
;
a
sio:SIO_001122
.
}
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_provenance
{
dgn-np:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_assertion
dcterms:description
"[While the study has several limitations, the results are consistent with a growing body of literature that suggests that the pharmacogenetics of depression (an inherently complex disorder) may turn out to be multifactorial, and may include the HTR1A gene in concert with other serotonin-related genes.]. 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:17570737
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}