@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0
> .
@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/v4.0.0/void/
> .
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_head
{
this:
np:hasAssertion
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_assertion
;
np:hasProvenance
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_assertion
a
np:Assertion
.
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_provenance
a
np:Provenance
.
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_assertion
{
miriam-gene:6323
a
ncit:C16612
.
lld:C0014550
a
ncit:C7057
.
dgn-gda:DGN658ab5eff562c58503b49e947c8e0c88
sio:SIO_000628
miriam-gene:6323
,
lld:C0014550
;
a
sio:SIO_001122
.
}
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_provenance
{
dgn-np:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_assertion
dcterms:description
"[Typical Severe Myoclonic Epilepsy (SME) and Borderline SME show distinct differences in photoparoxysmal response and gender, which might be caused by some genetic mechanism (s) other than the SCN1A gene mutation.]. 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:13129592
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP201428.RAoHNv2D1p232fmjpzQDtAcFYYDH9ct_2RGxq1KUhriJ0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:18+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}