@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_assertion
;
np:hasProvenance
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_provenance
;
np:hasPublicationInfo
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_assertion
a
np:Assertion
.
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_provenance
a
np:Provenance
.
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_assertion
{
miriam-gene:2690
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN09eb86ccb5cc6d99b43f52a641cd5d8a
sio:SIO_000628
miriam-gene:2690
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_provenance
{
dgn-np:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_assertion
dcterms:description
"[Our findings suggest that the level of genetic loading may have a dose-dependent effect on cortical thinning in the right ACC and in the left paracingulate cortex and that cortical thinning in GHR subjects may represent neurodevelopmental alterations that result from genetic liability for schizophrenia.]. 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:22998933
;
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:NP709335.RA3CPnFR01k3q_m3zZJFqALS4wZnIoK-rWE6EcK_Pm-dA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}