@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k
> .
@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:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_head
{
this:
np:hasAssertion
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_assertion
;
np:hasProvenance
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_provenance
;
np:hasPublicationInfo
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_assertion
a
np:Assertion
.
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_provenance
a
np:Provenance
.
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_assertion
{
miriam-gene:6657
a
ncit:C16612
.
lld:C0014556
a
ncit:C7057
.
dgn-gda:DGNa957a8b615ab012c8091993804aab98c
sio:SIO_000628
miriam-gene:6657
,
lld:C0014556
;
a
sio:SIO_001121
.
}
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_provenance
{
dgn-np:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_assertion
dcterms:description
"[We searched for SOX2 mutation in 24 patients with typical hippocampal sclerosis and for common variations in SOX2 in 655 patients without eye disease but with epilepsy, including 91 patients with febrile seizures, 93 with hippocampal sclerosis, and 258 with 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:16529618
;
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:NP752837.RAcNDCXQlXX8jHpoPluVaDhAwL87pYDAHSHWRgBovMy6k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}