@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8
> .
@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:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_head
{
this:
np:hasAssertion
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_assertion
;
np:hasProvenance
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_provenance
;
np:hasPublicationInfo
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_assertion
a
np:Assertion
.
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_provenance
a
np:Provenance
.
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_assertion
{
miriam-gene:5817
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGNaacfe9a0ce1c29f20a59c2d800aa0752
sio:SIO_000628
miriam-gene:5817
,
lld:C0002895
;
a
sio:SIO_001121
.
}
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_provenance
{
dgn-np:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_assertion
dcterms:description
"[We investigated inducibility of life-threatening arrhythmias with programmed ventricular stimulation (PVS) in relation to clinical markers of sudden cardiac death (SCD) in subjects with hypertrophic cardiomyopathy (HCM) attributable to the Asp175Asn mutation in the alpha-tropomyosin gene (TPM1-Asp175Asn).]. 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:14734051
;
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:NP492476.RAXroVtk4Q22WUyQY52DZyUI7fG956I1h3vNW4QJ9T3j8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}