@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4
> .
@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:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_head
{
this:
np:hasAssertion
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_assertion
;
np:hasProvenance
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_provenance
;
np:hasPublicationInfo
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_assertion
a
np:Assertion
.
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_provenance
a
np:Provenance
.
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_assertion
{
miriam-gene:6335
a
ncit:C16612
.
lld:C0014805
a
ncit:C7057
.
dgn-gda:DGN79b6773300d73bfc522e4b0f9c69a521
sio:SIO_000628
miriam-gene:6335
,
lld:C0014805
;
a
sio:SIO_001121
.
}
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_provenance
{
dgn-np:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_assertion
dcterms:description
"[To elucidate the rate of missense mutations in the SCN9A gene (which encodes sodium channel Na(v)1.7) (OMIM 603415) among patients with primary erythermalgia and to examine the possibility that other sodium channels can cause the disease.]. 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:18347287
;
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:NP539454.RA2tKHIH5nEBSd9VuQAh3xPVyIm93QGFGSEmft9oU6Vx4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}