@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU
> .
@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:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_head
{
this:
np:hasAssertion
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion
;
np:hasProvenance
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_provenance
;
np:hasPublicationInfo
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion
a
np:Assertion
.
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_provenance
a
np:Provenance
.
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion
{
miriam-gene:3784
a
ncit:C16612
.
lld:C0038644
a
ncit:C7057
.
dgn-gda:DGN115c0796284d985caeb90b92d57df5bf
sio:SIO_000628
miriam-gene:3784
,
lld:C0038644
;
a
sio:SIO_001121
.
}
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_provenance
{
dgn-np:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_assertion
dcterms:description
"[The LQTS is caused by mutations in genes encoding cardiac ion channels, and mutations in the genes KVLQT1 and SCNA5 have been identified in cases initially diagnosed as SIDS, in addition to several polymorphisms in these 2 genes and in the HERG gene.]. 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:15466077
;
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:NP366819.RA_LRPeRYfYInye51XZYaV4eOkqxBfsIrEUnOgHYPxUSU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:34+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" .
}