@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18
> .
@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:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_head
{
this:
np:hasAssertion
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_assertion
;
np:hasProvenance
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_provenance
;
np:hasPublicationInfo
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_assertion
a
np:Assertion
.
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_provenance
a
np:Provenance
.
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_assertion
{
miriam-gene:5428
a
ncit:C16612
.
lld:C0007795
a
ncit:C7057
.
dgn-gda:DGN9663a070b77dabf71c3a6492e42bb343
sio:SIO_000628
miriam-gene:5428
,
lld:C0007795
;
a
sio:SIO_001121
.
}
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_provenance
{
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_assertion
dcterms:description
"[Our data support an emerging proposal that POLG gene testing should be considered in any child or adolescent who presents or develops intractable seizures with or without status epilepticus or epilepsia partialis continua, particularly when there is a history of psychomotor regression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:20138553
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP26498.RAHwrZ-JN5BRcVo1kLqOKRf_3A7Y8_fTrazSq99_uG_18130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:11+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" .
}