@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4
> .
@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 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#
> .
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{
this:
np:hasAssertion
dgn-np:NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4130_assertion
a
np:Assertion
.
dgn-np:NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4130_provenance
a
np:Provenance
.
dgn-np:NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:80314
a
ncit:C16612
.
lld:C0033953
a
ncit:C7057
.
dgn-gda:DGNd80709b05bfea9a03730e4b880d7f4e2
sio:SIO_000628
miriam-gene:80314
,
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;
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.
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dgn-np:NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4130_provenance
{
dgn-np:NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4130_assertion
dc:description
"[We report the first GWAS of FSD symptoms in humans. This has pointed to several `risk alleles` and the implication of the serotonin and GABA pathways. Ultimately, understanding key mechanisms via this research may lead to new FSD treatments and inform clinical practice and developments in psychiatric nosology.]. 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:22509378
;
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 .
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dgn-np:NP97066.RAVvRrje7RSOIU89EGDNQFBWpypL5YqGEBwkAOUxCQ8t4130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:49+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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