@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM
> .
@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:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_head
{
this:
np:hasAssertion
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_assertion
;
np:hasProvenance
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_provenance
;
np:hasPublicationInfo
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_assertion
a
np:Assertion
.
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_provenance
a
np:Provenance
.
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C0740898
a
ncit:C7057
.
dgn-gda:DGNcf79ad26c83e5c152e2e61a68aaabc6f
sio:SIO_000628
miriam-gene:6559
,
lld:C0740898
;
a
sio:SIO_001121
.
}
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_provenance
{
dgn-np:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_assertion
dcterms:description
"[Gitelman's syndrome is a hereditary disorder occurring due to loss of functional mutations of the gene encoding the distal convoluted tubule sodium chloride cotransporter (NCCT) and is characterized by hypokalemic metabolic alkalosis, hypomagnesemia and hypocalciuria.]. 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:19356345
;
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:NP356641.RAXiFcWxk-GH2k2sxwtjkOiTFGrz9i75LDhxOpZol9UpM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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" .
}