@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c
> .
@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:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_head
{
this:
np:hasAssertion
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_assertion
;
np:hasProvenance
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_provenance
;
np:hasPublicationInfo
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_assertion
a
np:Assertion
.
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_provenance
a
np:Provenance
.
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_assertion
{
miriam-gene:6323
a
ncit:C16612
.
lld:C0311335
a
ncit:C7057
.
dgn-gda:DGN3e83b30aa0474789d1c54fb41e950b0d
sio:SIO_000628
miriam-gene:6323
,
lld:C0311335
;
a
sio:SIO_001121
.
}
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_provenance
{
dgn-np:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_assertion
dcterms:description
"[The purpose of this study is to correlate different types of SCN1A mutations and (1) seizure control, (2) occurrence of convulsive status epilepticus (cSE), and (3) the presence of crouch gait in adult patients.]. 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:22780858
;
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:NP682483.RAv9eXynQgXfazCHYgr1r6bw4xd02v5jQeQAafr2mKC5c130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:31+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" .
}