@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg
> .
@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:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_head
{
this:
np:hasAssertion
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_assertion
;
np:hasProvenance
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_provenance
;
np:hasPublicationInfo
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_assertion
a
np:Assertion
.
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_provenance
a
np:Provenance
.
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_assertion
{
miriam-gene:2904
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN594fb864745037efeb35363588c7c379
sio:SIO_000628
miriam-gene:2904
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_provenance
{
dgn-np:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_assertion
dcterms:description
"[Because of the known role of the GRIN2B C2664T polymorphism in HD neuropathology, which is partly due to increased glutamatergic neural transmission, we analyze how this polymorphism influences error processing and response inhibition in a sample of healthy probands (N=65).]. 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:20399867
;
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:NP679465.RAwG4Ns2uvC7gtlIxe7faPj914DSfaKaB5Khltid8O6Bg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:50+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" .
}