@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI
> .
@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:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_head
{
this:
np:hasAssertion
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_assertion
;
np:hasProvenance
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_provenance
;
np:hasPublicationInfo
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_assertion
a
np:Assertion
.
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_provenance
a
np:Provenance
.
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_assertion
{
miriam-gene:6319
a
ncit:C16612
.
lld:C0878544
a
ncit:C7057
.
dgn-gda:DGN0d7ded52edf52808c04852304c47247c
sio:SIO_000628
miriam-gene:6319
,
lld:C0878544
;
a
sio:SIO_001121
.
}
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_provenance
{
dgn-np:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_assertion
dcterms:description
"[While in the older populations, SCD is most frequently caused by underlying coronary artery disease and heart failure, in those aged under 40 years, the causes of SCD commonly include genetic disorders, such as inherited cardiomyopathies and primary arrhythmogenic diseases.]. 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:21816129
;
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:NP668278.RAbX-rHpXgmVeWWtTWBhJw9gZNfsOJYtHykX1o2T4AvkI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:43+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" .
}