@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs
> .
@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:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_head
{
this:
np:hasAssertion
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_assertion
;
np:hasProvenance
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_provenance
;
np:hasPublicationInfo
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_assertion
a
np:Assertion
.
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_provenance
a
np:Provenance
.
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_assertion
{
miriam-gene:6584
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN81cbf4cbf8018017b4d6190581629c8b
sio:SIO_000628
miriam-gene:6584
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_provenance
{
dgn-np:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_assertion
dcterms:description
"[It is becoming increasingly appreciated that besides depressed left ventricular systolic function and the conventional risk stratification tools, new markers for plaque vulnerability, enhanced thrombogenesis, specific genetic alterations of the autonomic nervous system, cardiac sarcolemmal and contractile proteins, and familial clustering may better segregate patients with atherosclerotic coronary artery disease who are at high risk for SCD from those who may suffer from nonfatal ischemic events.]. 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:14521667
;
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:NP330063.RAz0VnIP89zTZUy3A-s-ZiVptE1KKcydqGr7XHHNDKHqs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}