@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg
> .
@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:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_head
{
this:
np:hasAssertion
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_assertion
;
np:hasProvenance
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_provenance
;
np:hasPublicationInfo
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_assertion
a
np:Assertion
.
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_provenance
a
np:Provenance
.
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_assertion
{
miriam-gene:6584
a
ncit:C16612
.
lld:C0039070
a
ncit:C7057
.
dgn-gda:DGNc4cd11516992c630536e8b83bb88ed65
sio:SIO_000628
miriam-gene:6584
,
lld:C0039070
;
a
sio:SIO_001121
.
}
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_provenance
{
dgn-np:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_assertion
dcterms:description
"[Although SCD may be the first presentation of arrhythmic syndromes, patients may present to the general physician with symptoms of palpitations or hemodynamic compromise, including dizziness, seizure, or syncope, particularly following exertion.]. 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:23651009
;
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:NP194204.RARPKTTgnyHw9aeGXpZkqK_2NWIseAydtFjiA8ODFEUrg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}