@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ
> .
@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:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_head
{
this:
np:hasAssertion
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_assertion
;
np:hasProvenance
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_assertion
a
np:Assertion
.
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_provenance
a
np:Provenance
.
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_assertion
{
miriam-gene:6340
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN1492e516989a9f510fb89d20b2595d2f
sio:SIO_000628
miriam-gene:6340
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_provenance
{
dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_assertion
dcterms:description
"[The roles of these missense mutations in the SCNN1B or SCNN1G gene identified in hypertensive patients are not clear in the pathogenesis of hypertension and the regulation of electrolytes. Thus, further investigation of these mutations, including functional analyses, will be needed.]. 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:15198480
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}