@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY
> .
@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:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_head
{
this:
np:hasAssertion
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_assertion
;
np:hasProvenance
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_provenance
;
np:hasPublicationInfo
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_assertion
a
np:Assertion
.
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_provenance
a
np:Provenance
.
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C1845202
a
ncit:C7057
.
dgn-gda:DGNd1f0955f484652d6bbeb16379138396a
sio:SIO_000628
miriam-gene:551
,
lld:C1845202
;
a
sio:SIO_001121
.
}
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_provenance
{
dgn-np:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_assertion
dcterms:description
"[Our results indicate that NSIAD is already present during the neonatal period and that molecular analysis of the V2R receptor should therefore be carried out, in all newborns with prolonged euvolemic hyponatremia with hypo-osmolarity, high urinary sodium and normal/low or undetectable AVP 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:18622631
;
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:NP809701.RA_pCgtYFjFb5wElVv9X9QPJFhDwZSoLZCWJyf01BwrPY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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: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" .
}