@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU
> .
@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:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_head
{
this:
np:hasAssertion
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_assertion
;
np:hasProvenance
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_provenance
;
np:hasPublicationInfo
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_assertion
a
np:Assertion
.
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_provenance
a
np:Provenance
.
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_assertion
{
miriam-gene:2902
a
ncit:C16612
.
lld:C0014556
a
ncit:C7057
.
dgn-gda:DGNe9a51ed1270a07cb889fc9cac6309f2e
sio:SIO_000628
miriam-gene:2902
,
lld:C0014556
;
a
sio:SIO_001121
.
}
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_provenance
{
dgn-np:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_assertion
dcterms:description
"[We have investigated whether human temporal lobe epilepsy is associated with changes in the NMDA receptor at the molecular level by assessing the relative expression of mRNAs of the different splice variants at the N-terminal (exon 5) and C-terminal (exon 21) position for the NMDAR1 subunit.]. 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:10762714
;
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:NP532217.RAnucFqgw5ORwH9Nuqi6GSne7DQtsfjuuSc_1wVzYLQvU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}