@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_head
{
this:
np:hasAssertion
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_assertion
;
np:hasProvenance
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_assertion
a
np:Assertion
.
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_provenance
a
np:Provenance
.
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_assertion
{
miriam-gene:6657
a
ncit:C16612
.
lld:C0009952
a
ncit:C7057
.
dgn-gda:DGNa5cf6b8320c1c361f7dc766febb1e712
sio:SIO_000628
miriam-gene:6657
,
lld:C0009952
;
a
sio:SIO_001121
.
}
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_provenance
{
dgn-np:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_assertion
dcterms:description
"[However, although mutation of SOX2 in humans causes hippocampal malformation, SOX2 mutation or variation is unlikely to contribute commonly to mesial temporal lobe epilepsy or its structural (hippocampal sclerosis) or historic (febrile seizures) associations in humans.]. 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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP707992.RAbqu2PpYUL_fJyD77VHRM6psvMxNYClQHIUD9mZXVv0Q130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:47+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}