@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U
> .
@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:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_head
{
this:
np:hasAssertion
dgn-np:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_publicationInfo
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.
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dgn-np:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_assertion
{
miriam-gene:27129
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGN6cb2dcac3aeb75814b85f2dfd8e4681e
sio:SIO_000628
miriam-gene:27129
,
lld:C0018801
;
a
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.
}
dgn-np:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_provenance
{
dgn-np:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_assertion
dcterms:description
"[Of 51 exonic CLCNKA variants identified, one SNP (rs10927887, encoding Arg83Gly) was common, in linkage disequilibrium with the heart failure risk SNP in HSPB7, and associated with heart failure in two independent Caucasian referral populations (n = 2,606 and 1,168; combined P = 2.25 × 10(-6)).]. 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:21248228
;
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:NP866370.RAFoKz7GAXLwIpTtHcXtuinPiHvhIjSjq-MKgaZWLGW1U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:17+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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
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"v4.0.0" .
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