@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q
> .
@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:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_head
{
this:
np:hasAssertion
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_assertion
;
np:hasProvenance
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_assertion
a
np:Assertion
.
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_provenance
a
np:Provenance
.
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_assertion
{
miriam-gene:2913
a
ncit:C16612
.
lld:C0679466
a
ncit:C7057
.
dgn-gda:DGN4d001c374189ebe8589407e81dea04d3
sio:SIO_000628
miriam-gene:2913
,
lld:C0679466
;
a
sio:SIO_001121
.
}
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_provenance
{
dgn-np:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_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:NP512297.RAF9YE1wvwvjVE7J86CPDd_sE2NJwLa2CUMlg6P5__z2Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}