@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74
> .
@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:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_head
{
this:
np:hasAssertion
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_assertion
;
np:hasProvenance
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_provenance
;
np:hasPublicationInfo
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_assertion
a
np:Assertion
.
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_provenance
a
np:Provenance
.
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_assertion
{
miriam-gene:6329
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN064786c31ba1cea0d60a6ec9ee2c6175
sio:SIO_000628
miriam-gene:6329
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_provenance
{
dgn-np:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_assertion
dcterms:description
"[The present study is to observe in vitro the proliferation ability of the muscle cells from permanent myopathy (PM) patients of nomokalaemic periodic paralysis (normKPP), which is caused by mutations of Met1592Val in the skeletal muscle voltage gated sodium channel (SCN4A) gene on chromosome 17q23.1.]. 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:19290024
;
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:NP791054.RAKyKqBuzzUKy4ywtdurWwNTSaCeUx0TNCKtSC2oXnh74130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}