@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI
> .
@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:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_head
{
this:
np:hasAssertion
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_assertion
;
np:hasProvenance
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_provenance
;
np:hasPublicationInfo
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_assertion
a
np:Assertion
.
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_provenance
a
np:Provenance
.
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNffe81e3276f3d2d439746a76f4c6ec23
sio:SIO_000628
miriam-gene:5621
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_provenance
{
dgn-np:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_assertion
dcterms:description
"[Ablation of the cellular prion protein (PrP(c)) gene (PRNP) enhances neuronal excitability of the hippocampus in vitro and sensitivity to seizure in vivo, indicating that PrP(c) might be related to epilepsy.]. 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:14610121
;
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:NP606588.RAtXXRYEtvfmrEmx_CAKD2viERgfqne4iqWf5MlCAwgsI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}