@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU
> .
@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:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_head
{
this:
np:hasAssertion
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_assertion
;
np:hasProvenance
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_provenance
;
np:hasPublicationInfo
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_assertion
a
np:Assertion
.
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_provenance
a
np:Provenance
.
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0236792
a
ncit:C7057
.
dgn-gda:DGN6ad661d1118320948f129f971cf81eed
sio:SIO_000628
miriam-gene:6532
,
lld:C0236792
;
a
sio:SIO_001121
.
}
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_provenance
{
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_assertion
dcterms:description
"[As two individuals with SERT I425V and OCD also had Asperger syndrome (AS), an autism spectrum disorder, and as other rare SERT variants have recently shown significant associations with autism, we set out to extend our original OCD study by genotyping additional autism/AS and OCD samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:18197083
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:13+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" .
}