@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk
> .
@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:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_head
{
this:
np:hasAssertion
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_assertion
;
np:hasProvenance
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_provenance
;
np:hasPublicationInfo
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_assertion
a
np:Assertion
.
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_provenance
a
np:Provenance
.
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_assertion
{
miriam-gene:54820
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN50a025ecc7004e8fd633ce6133e37dc6
sio:SIO_000628
miriam-gene:54820
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_provenance
{
dgn-np:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_assertion
dcterms:description
"[We found that apart from a 3 mm hamartia in the temporal cortex of one MTLE case with NDE1 deletion and known hippocampal sclerosis in the other case, cortical lamination and cytoarchitecture were normal, with no differences between cases with deletion and disease controls.]. 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:22523559
;
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:NP544751.RAcEL33SQzhD0ujw2f6NvZNf4LCYGlbYUmXwCFwj-5zxk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:28+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" .
}