@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs
> .
@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:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_head
{
this:
np:hasAssertion
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_assertion
;
np:hasProvenance
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_assertion
a
np:Assertion
.
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_provenance
a
np:Provenance
.
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0033805
a
ncit:C7057
.
dgn-gda:DGN793423725c985a874dfb201cdc675e8b
sio:SIO_000628
miriam-gene:5972
,
lld:C0033805
;
a
sio:SIO_001121
.
}
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_provenance
{
dgn-np:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_assertion
dcterms:description
"[Pseudohypoaldosteronism (PHA) is characterized by salt-wasting and failure to thrive in the newborn, accompanied by high urinary levels of sodium despite hyponatremia, hyperkalemia and metabolic acidosis, elevation of plasma renin activity, and high plasma aldosterone levels.]. 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:7792806
;
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:NP819908.RAt_S7QURI_NYHhnbQlK42uxBnq2vsdLtKfajr0nWbfZs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:22+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" .
}