@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0
> .
@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:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_head
{
this:
np:hasAssertion
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_assertion
;
np:hasProvenance
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_provenance
;
np:hasPublicationInfo
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_assertion
a
np:Assertion
.
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_provenance
a
np:Provenance
.
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_assertion
{
miriam-gene:5578
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN1212f1815ed878bab99132c466f0ae7e
sio:SIO_000628
miriam-gene:5578
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_provenance
{
dgn-np:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_assertion
dcterms:description
"[Three polymorphisms (GRIN2B rs220599, GRM3 rs2189814 and PRKCA rs8074995) were associated with episodic verbal memory in both control and patients with cognitive deficit, but not in cognitively spared patients or the pooled schizophrenia sample.]. 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:21281445
;
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:NP357227.RA8oiVoOKyMH3TxXJ0A4XXURiBG5Wjm6D_MULtoTwQ9W0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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" .
}