@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc
> .
@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:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_head
{
this:
np:hasAssertion
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_assertion
;
np:hasProvenance
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_provenance
;
np:hasPublicationInfo
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_assertion
a
np:Assertion
.
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_provenance
a
np:Provenance
.
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_assertion
{
miriam-gene:952
a
ncit:C16612
.
lld:C1848140
a
ncit:C7057
.
dgn-gda:DGN4175f2a8d52cc327b55f75ef6ae16e35
sio:SIO_000628
miriam-gene:952
,
lld:C1848140
;
a
sio:SIO_001121
.
}
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_provenance
{
dgn-np:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_assertion
dcterms:description
"[Animal models with genetic alterations of the OT system, like the OT, OT receptor and CD38 knock-out mice, and those with phenotypic variation in social behavior, like BTBR inbred mice and prairie voles, coupled with behavioral paradigms with face and construct validity may prove to have predictive validity for identifying the most efficacious methods of stimulating the OT system to enhance social cognition in humans.]. 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:22206823
;
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:NP880743.RAYFsab0jrVij6OeW5NMDTV42K8oKuS5ECkUVRm4-LtEc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}