@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc
> .
@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:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_head
{
this:
np:hasAssertion
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_assertion
;
np:hasProvenance
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_provenance
;
np:hasPublicationInfo
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_assertion
a
np:Assertion
.
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_provenance
a
np:Provenance
.
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C0741923
a
ncit:C7057
.
dgn-gda:DGN9484458b2e6c630277f5c81ebd04394c
sio:SIO_000628
miriam-gene:3757
,
lld:C0741923
;
a
sio:SIO_001121
.
}
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_provenance
{
dgn-np:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_assertion
dcterms:description
"[In 118 genetically-confirmed LQT2 patients (69 families, 62 KCNH2 mutations), the ECG parameters, Schwartz scores, and the incidence of cardiac events, defined as syncope, aborted cardiac arrest, and sudden cardiac death, were evaluated.]. 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:18441445
;
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:NP277974.RASEsCFaItXUyxC454VHNpLP3gB0SoMIrRQsBV1CJB0yc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:36+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" .
}