@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58
> .
@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:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_head
{
this:
np:hasAssertion
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_assertion
;
np:hasProvenance
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_provenance
;
np:hasPublicationInfo
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_assertion
a
np:Assertion
.
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_provenance
a
np:Provenance
.
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_assertion
{
miriam-gene:8831
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGNaafa37751418c65ab5d9b0ed7a5a1495
sio:SIO_000628
miriam-gene:8831
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_provenance
{
dgn-np:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_assertion
dcterms:description
"[In addition, experimental evidence that SYNGAP1 and CuTA are involved in the secretory pathway in neurons, through glutamate and acetylcholinesterase signalling, prompted us to consider modulation of the glutamate pathway as target of a therapeutic strategy for seizure control.]. 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:21119708
;
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:NP429233.RA2_JFjAtKBskf_RSt2t7lA4EccOPbVKO5rI8WvAc8O58130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}