@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I
> .
@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:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_head
{
this:
np:hasAssertion
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_assertion
;
np:hasProvenance
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_provenance
;
np:hasPublicationInfo
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_assertion
a
np:Assertion
.
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_provenance
a
np:Provenance
.
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_assertion
{
miriam-gene:6261
a
ncit:C16612
.
lld:C0009917
a
ncit:C7057
.
dgn-gda:DGN8d6c129fb40d226798d198d3be3b10bd
sio:SIO_000628
miriam-gene:6261
,
lld:C0009917
;
a
sio:SIO_001121
.
}
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_provenance
{
dgn-np:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_assertion
dcterms:description
"[The differences between the groups in the halothane and caffeine IVCT threshold concentrations and in the time course of contracture development in the ryanodine IVCT underline the hypothesis that certain mutations in the RYR1 gene could make the ryanodine receptor more sensitive to specific ligands.]. 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:12151923
;
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:NP354640.RAB46Kp8227bOUVs_ENzt21QJa03zNCOQQ8bxi-k47a7I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}