@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY
> .
@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:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_head
{
this:
np:hasAssertion
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_assertion
;
np:hasProvenance
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_provenance
;
np:hasPublicationInfo
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_assertion
a
np:Assertion
.
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_provenance
a
np:Provenance
.
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_assertion
{
miriam-gene:6635
a
ncit:C16612
.
lld:C0751122
a
ncit:C7057
.
dgn-gda:DGNfd3a44c4b650d7422282f6ab340f13a1
sio:SIO_000628
miriam-gene:6635
,
lld:C0751122
;
a
sio:SIO_001121
.
}
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_provenance
{
dgn-np:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_assertion
dcterms:description
"[It is thought that patients with both TSME and BSME have some predisposition toward paroxysmal movement disorders, and that this predisposition is partly related to sodium channel dysfunction, although some other factors might influence the occurrence of this phenomenon.]. 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:12907273
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP809876.RAxL1tJjJFC4ll97ErIhFxxjvavBDrF045tbmBGPhQYTY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}