@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM
> .
@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:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_head
{
this:
np:hasAssertion
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_assertion
;
np:hasProvenance
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_provenance
;
np:hasPublicationInfo
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_assertion
a
np:Assertion
.
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_provenance
a
np:Provenance
.
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_assertion
{
miriam-gene:5021
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN46907079291a580ac89ef8f6af9409e5
sio:SIO_000628
miriam-gene:5021
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_provenance
{
dgn-np:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_assertion
dcterms:description
"[Together, these data provide further evidence for the role of OXTR and the oxytocin signaling pathway in the etiology of autism and, for the first time, implicate the epigenetic regulation of OXTR in the development of the disorder.See the related commentary by Gurrieri and Neri: http://www.biomedcentral.com/1741-7015/7/63.]. 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:19845972
;
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:NP453370.RAwHKuU449aP2cEif_4v_Z4bfByIRZ-2FXnQ_PaDb42zM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:30+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" .
}