@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts
> .
@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:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_head
{
this:
np:hasAssertion
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_assertion
;
np:hasProvenance
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_provenance
;
np:hasPublicationInfo
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_assertion
a
np:Assertion
.
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_provenance
a
np:Provenance
.
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_assertion
{
miriam-gene:4535
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGN6a62628dfe7f6228db13d5e3a65219a7
sio:SIO_000628
miriam-gene:4535
,
lld:C0023976
;
a
sio:SIO_001121
.
}
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_provenance
{
dgn-np:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_assertion
dcterms:description
"[Therefore, we stated that the 3394 mutation in the ND1 gene is pathogenic and could be the cause of prolongation of the QTU intervals or modification of the phenotypes of not only congenital but also so-called acquired drug-induced long QT syndrome.]. 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:10092538
;
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:NP248529.RAulI5LTnqRoH6zunrosTJoFwA8rQwLTWCKiDuLCk-Rts130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:38+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" .
}