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http://rdf.disgenet.org/nanopublications.trig#NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8
> .
@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:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_head
{
this:
np:hasAssertion
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_assertion
;
np:hasProvenance
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance
;
np:hasPublicationInfo
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_assertion
a
np:Assertion
.
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance
a
np:Provenance
.
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0004775
a
ncit:C7057
.
dgn-gda:DGNdc988de3180bc4f1b966056be75e9019
sio:SIO_000628
miriam-gene:5972
,
lld:C0004775
;
a
sio:SIO_001121
.
}
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_provenance
{
dgn-np:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_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-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:NP775241.RASsg4mASj69ne1irsPbSMHDLekoIvs633p1ZeO4MHDT8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:49+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" .
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pav:version
"v2.1.0" .
}