@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw
> .
@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:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_head
{
this:
np:hasAssertion
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_assertion
;
np:hasProvenance
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_assertion
a
np:Assertion
.
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_provenance
a
np:Provenance
.
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_assertion
{
miriam-gene:100128922
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN6a7a493a545c875c1cdf536b38850539
sio:SIO_000628
miriam-gene:100128922
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_provenance
{
dgn-np:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_assertion
dcterms:description
"[These findings indicate that there is an increase in the level of connexin mRNA in the temporal cortex of patients exhibiting seizure disorders, suggesting an increase in the synthesis of gap junction protein that may lead to an increase in intercellular coupling.]. 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:1846600
;
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:NP915957.RAEkMYmCxclukYkTSZLP5Aq1bCRfWrJeV7SmqiiMs3Aqw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}