@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8
> .
@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:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_head
{
this:
np:hasAssertion
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_assertion
;
np:hasProvenance
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_provenance
;
np:hasPublicationInfo
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_assertion
a
np:Assertion
.
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_provenance
a
np:Provenance
.
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_assertion
{
miriam-gene:6323
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN310d085feba0d1b40809ab9e79855945
sio:SIO_000628
miriam-gene:6323
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_provenance
{
dgn-np:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_assertion
dcterms:description
"[It can also be argued that because of striking clinical resemblance between Dravet and various epileptic and encephalopathic syndromes associated with SCN1A gene mutations and SSPE, SCN1A gene abnormalities may also be responsible for susceptibility to SSPE in measles infected children.]. 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:22098725
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP940040.RAwGoeVa1gfdYtEVuQcd1czuyRLgm3vpBODc-uoIk60a8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:51+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" .
}