@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w
> .
@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:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_head
{
this:
np:hasAssertion
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_assertion
;
np:hasProvenance
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_provenance
;
np:hasPublicationInfo
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_assertion
a
np:Assertion
.
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_provenance
a
np:Provenance
.
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_assertion
{
miriam-gene:5021
a
ncit:C16612
.
lld:C0003469
a
ncit:C7057
.
dgn-gda:DGN7dc67a8d7d8f2bafd5bcade4f68da4fa
sio:SIO_000628
miriam-gene:5021
,
lld:C0003469
;
a
sio:SIO_001121
.
}
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_provenance
{
dgn-np:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_assertion
dcterms:description
"[It is suggested that polymorphic variation at the oxytocin receptor gene (rs2254298) is associated with sociability, amygdala volume and differential risk for psychiatric conditions including autism, depression and anxiety disorder, depending on the quality of early environmental experiences.]. 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:22510359
;
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:NP667463.RATWq97VDlXoe24iMHxD4vBKmEELtBhYl_OXloCBLuf7w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:43+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" .
}