@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k
> .
@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:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_head
{
this:
np:hasAssertion
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_assertion
;
np:hasProvenance
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_provenance
;
np:hasPublicationInfo
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_assertion
a
np:Assertion
.
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_provenance
a
np:Provenance
.
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_assertion
{
miriam-gene:3753
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN9155babfc7163d0230e03bbc922bc2f0
sio:SIO_000628
miriam-gene:3753
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_provenance
{
dgn-np:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_assertion
dcterms:description
"[This suggests that genetic determinants located in KCNQ1, KCNE1, KCNH2 and SCN5A influence QTc length in healthy individuals and may represent risk factors for arrhythmias or cardiac sudden death in patients with cardiovascular diseases.]. 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:16132053
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP123728.RAvHg7Ley27FA9eriJY9-0fdxKytIuLay_phX9V_LPf_k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:04+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" .
}