@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_head
{
this:
np:hasAssertion
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_assertion
;
np:hasProvenance
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_provenance
;
np:hasPublicationInfo
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_assertion
a
np:Assertion
.
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_provenance
a
np:Provenance
.
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C1141890
a
ncit:C7057
.
dgn-gda:DGNf6dac22cab3e5fb8745da9ddf8a3fbf2
sio:SIO_000628
miriam-gene:6331
,
lld:C1141890
;
a
sio:SIO_001121
.
}
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_provenance
{
dgn-np:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_assertion
dcterms:description
"[Congenital long-QT syndrome (LQTS) is caused by mutations of genes encoding the slow component of the delayed rectifier current (LQT1, LQT5), the rapid component of the delayed rectifier current (LQT2, LQT6), or the Na(+) current (LQT3), resulting in ST-T-wave abnormalities on the ECG.]. 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:11104743
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP302074.RAqjRSKhn0NOj-M2m20rKrBK9wJnZs44qXqepKyJMEwfE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:02+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}