@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08
> .
@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:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_head
{
this:
np:hasAssertion
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_assertion
;
np:hasProvenance
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_provenance
;
np:hasPublicationInfo
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_assertion
a
np:Assertion
.
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_provenance
a
np:Provenance
.
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_assertion
{
miriam-gene:6319
a
ncit:C16612
.
lld:C0152021
a
ncit:C7057
.
dgn-gda:DGNad1e9b33175fdca7595587918a25c2eb
sio:SIO_000628
miriam-gene:6319
,
lld:C0152021
;
a
sio:SIO_001121
.
}
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_provenance
{
dgn-np:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_assertion
dcterms:description
"[The study of SCD has focused on several major themes: progress in understanding the causes and treatments of genetic cardiovascular diseases, improved management of patients with congenital heart disease with SCD risk, treatment strategies for SCD risk reduction in patients with cardiomyopathies, and defining guidelines for athletic preparticipation screening.]. 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:18781113
;
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:NP468950.RAmkrVD4MU46zIUMg7NHzPYlzLr6LRkrnAp1V-I6mcf08130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}