@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak
> .
@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:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_head
{
this:
np:hasAssertion
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_assertion
;
np:hasProvenance
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_provenance
;
np:hasPublicationInfo
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_assertion
a
np:Assertion
.
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_provenance
a
np:Provenance
.
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_assertion
{
miriam-gene:132
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNcb0ddc7f91e4a29fa69e27cb321594e1
sio:SIO_000628
miriam-gene:132
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_provenance
{
dgn-np:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_assertion
dcterms:description
"[Importantly, ADK was found to be overexpressed and associated with astrogliosis and spontaneous seizures in rodent models of epilepsy, as well as in human specimen resected from patients with hippocampal sclerosis and temporal lobe 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:22700220
;
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:NP280729.RAcecLRmXTt3qxX-XEBsJmdquyfRiU2pqbUTbLng3cwak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}