@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM
> .
@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:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_head
{
this:
np:hasAssertion
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_assertion
;
np:hasProvenance
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_provenance
;
np:hasPublicationInfo
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_assertion
a
np:Assertion
.
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_provenance
a
np:Provenance
.
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_assertion
{
miriam-gene:43
a
ncit:C16612
.
lld:C0036391
a
ncit:C7057
.
dgn-gda:DGN0e0d81cfe0112e2811cfd6051bb971ce
sio:SIO_000628
miriam-gene:43
,
lld:C0036391
;
a
sio:SIO_001121
.
}
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_provenance
{
dgn-np:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_assertion
dcterms:description
"[It has been suggested that SJS neuromyotonia may result from endplate acetylcholinesterase (AChE) deficiency, but this hypothesis has never been investigated in vivo due to the lack of an animal model for neuromyotonia.]. 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:18647752
;
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:NP166411.RA2e_Gs0LG_2Vz4iX2y_5gqbDv_qHpDELv0swJenHAkpM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}