@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU
> .
@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:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_head
{
this:
np:hasAssertion
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_assertion
;
np:hasProvenance
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_provenance
;
np:hasPublicationInfo
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_assertion
a
np:Assertion
.
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_provenance
a
np:Provenance
.
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_assertion
{
miriam-gene:6319
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGN4b774beddb0a66b109c9d4bcea051e25
sio:SIO_000628
miriam-gene:6319
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_provenance
{
dgn-np:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_assertion
dcterms:description
"[Although therapy for monomorphic VT associated with structural heart disease focuses on tachycardia suppression and reduction of sudden cardiac death (SCD) risk, idiopathic monomorphic VT generally does not entail an increased risk of SCD and treatment is aimed primarily at symptom reduction.]. 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:20887902
;
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:NP181901.RAkOtrZloQadhPqiG1-ccxd9QmSKxshwfHJmRVgYF5IEU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}