@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c
> .
@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:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_head
{
this:
np:hasAssertion
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_assertion
;
np:hasProvenance
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_provenance
;
np:hasPublicationInfo
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_assertion
a
np:Assertion
.
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_provenance
a
np:Provenance
.
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_assertion
{
miriam-gene:5817
a
ncit:C16612
.
lld:C0007194
a
ncit:C7057
.
dgn-gda:DGNa0af0ae6c54acca73b5f1a08c696b047
sio:SIO_000628
miriam-gene:5817
,
lld:C0007194
;
a
sio:SIO_001121
.
}
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_provenance
{
dgn-np:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_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:NP742948.RAiFlGSE_PHyC8CvyjTihGrNKbn17u6ZDNPqk_Gvpmk7c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}