@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8
> .
@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:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_head
{
this:
np:hasAssertion
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_assertion
;
np:hasProvenance
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_provenance
;
np:hasPublicationInfo
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_assertion
a
np:Assertion
.
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_provenance
a
np:Provenance
.
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_assertion
{
miriam-gene:11169
a
ncit:C16612
.
lld:C0311335
a
ncit:C7057
.
dgn-gda:DGN87e68d00963567ea450795d567b699f7
sio:SIO_000628
miriam-gene:11169
,
lld:C0311335
;
a
sio:SIO_001121
.
}
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_provenance
{
dgn-np:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_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:NP861355.RAFcOKR2p74lKk01K7BBZp-xwp9695OdON6HkJdiHt5O8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:23+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" .
}