@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4
> .
@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/v3.0.0/void/
> .
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_head
{
this:
np:hasAssertion
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_assertion
;
np:hasProvenance
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_provenance
;
np:hasPublicationInfo
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_assertion
a
np:Assertion
.
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_provenance
a
np:Provenance
.
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGN79e0840c2c9441c831b978d712d118b2
sio:SIO_000628
miriam-gene:3767
,
lld:C0018802
;
a
sio:SIO_001122
.
}
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_provenance
{
dgn-np:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_assertion
dcterms:description
"[The Kir6.2 E23K polymorphism in DCM patients of Han ethnicity may increase the risk of negative outcomes such as congestive heart failure and sudden cardiac death by affecting LVEDD and LAD.]. 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:24222218
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP522675.RAMwRAdTlFNf-CUrqNGaZ_ciWci1X9Esp46d-hUqFRqO4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:49+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}