@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg
> .
@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:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_head
{
this:
np:hasAssertion
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_assertion
;
np:hasProvenance
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_assertion
a
np:Assertion
.
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_provenance
a
np:Provenance
.
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0740898
a
ncit:C7057
.
dgn-gda:DGN2474dde3a5b3853ca0661e03ffd9fc52
sio:SIO_000628
miriam-gene:5972
,
lld:C0740898
;
a
sio:SIO_001121
.
}
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_provenance
{
dgn-np:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_assertion
dcterms:description
"[Bartter syndrome, an autosomal recessive renal tubular disorder, is associated with hypokalemic metabolic alkalosis with high renin and aldosterone plasma concentrations with low or normal blood pressure and renal salt loss.]. 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:9502574
;
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:NP1390613.RAl8Q-0xUIj-LSkphWBMfXIN_s1_Rtt5-XCGf3Ph-Z-tg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}