@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA
> .
@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#
> .
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_head
{
this:
np:hasAssertion
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_assertion
;
np:hasProvenance
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_provenance
;
np:hasPublicationInfo
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_assertion
a
np:Assertion
.
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_provenance
a
np:Provenance
.
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_assertion
{
miriam-gene:3356
a
ncit:C16612
.
lld:C0028768
a
ncit:C7057
.
dgn-gda:DGN4dd04cf92d9b78dd5ce428e1b4c77459
sio:SIO_000628
miriam-gene:3356
,
lld:C0028768
;
a
sio:SIO_001122
.
}
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_provenance
{
dgn-np:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_assertion
dct:description
"[The results suggest that the C516T variant of the 5HT2A gene may be one of the genetic risk factors for OCD in our sample. However, further studies using larger samples and family based methods are recommended to confirm these findings.]. 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:15005715
;
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:NP57300.RA8u2lcNYRENpZf48tR2PnlOr2LP_WXWoNAJLBoTfO1RA130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:27+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}