@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg
> .
@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:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_head
{
this:
np:hasAssertion
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_assertion
;
np:hasProvenance
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_provenance
;
np:hasPublicationInfo
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_assertion
a
np:Assertion
.
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_provenance
a
np:Provenance
.
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_assertion
{
miriam-gene:1188
a
ncit:C16612
.
lld:C0268450
a
ncit:C7057
.
dgn-gda:DGN253853cbe732ed161247d7a07068e78c
sio:SIO_000628
miriam-gene:1188
,
lld:C0268450
;
a
sio:SIO_001121
.
}
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_provenance
{
dgn-np:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_assertion
dcterms:description
"[Inactivation mutations of the luminal thiazide-sensitive NaCl cotransporter (NCC) in the distal convoluted tubules or the basolateral chloride channel (CLCNKB) in the distal nephron are the most common genetic mutations in Gitelman's syndrome (GS) or Bartter's syndrome (BS).]. 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:15687331
;
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:NP576108.RAJjCKUkOfTDD61aGdCPSoMXfNTwqorMZT7X-XkuPHSYg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}