@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg
> .
@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:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_head
{
this:
np:hasAssertion
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_assertion
;
np:hasProvenance
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_assertion
a
np:Assertion
.
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_provenance
a
np:Provenance
.
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_assertion
{
miriam-gene:9211
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN8e96d6acf62db48525ea944a80c2ebdc
sio:SIO_000628
miriam-gene:9211
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_provenance
{
dgn-np:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_assertion
dcterms:description
"[These results suggest that the two protein isoforms encoded by LGI1/Epitempin are differentially expressed in the human brain, and that higher expression levels of these proteins in the lateral temporal cortex may underlie the susceptibility of this brain region to the epileptogenic effects of LGI1/Epitempin mutations.]. 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:16787412
;
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:NP741035.RADSjfym65uUjeGZ2_h8Ki0LavW2v6FEed3TxIdwT0qwg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}