@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A
> .
@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:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_head
{
this:
np:hasAssertion
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_assertion
;
np:hasProvenance
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_provenance
;
np:hasPublicationInfo
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_assertion
a
np:Assertion
.
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_provenance
a
np:Provenance
.
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_assertion
{
miriam-gene:3753
a
ncit:C16612
.
lld:C0232197
a
ncit:C7057
.
dgn-gda:DGN1cd23279b0b48d064ba68074c71a3c56
sio:SIO_000628
miriam-gene:3753
,
lld:C0232197
;
a
sio:SIO_001121
.
}
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_provenance
{
dgn-np:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_assertion
dcterms:description
"[These results further our understanding of the structural relationship between KCNE1 and KCNQ1 subunits in the I(Ks) channel, and provide mechanisms for understanding the effects on channel deactivation underlying these two atrial fibrillation mutations.]. 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:22250012
;
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:NP186631.RAfiD2hXNi7w9yyErKNVqSvYOIQtzuxGmVIXG8uOrZg0A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}