@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E
> .
@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:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_head
{
this:
np:hasAssertion
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_assertion
;
np:hasProvenance
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_provenance
;
np:hasPublicationInfo
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_assertion
a
np:Assertion
.
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_provenance
a
np:Provenance
.
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C1845202
a
ncit:C7057
.
dgn-gda:DGN8005848745ae6d0d2c32679872891edd
sio:SIO_000628
miriam-gene:7450
,
lld:C1845202
;
a
sio:SIO_001121
.
}
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_provenance
{
dgn-np:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_assertion
dcterms:description
"[We performed a stimulation test with 1-desamino-D arginin vasopressin (dDAVP) 0·3 μg/kg of bodyweight in three patients (two hemizygous male and one heterozygous female) with NSIAD with R137C mutation and measured on the one hand the levels of vWF and fVIII and the other hand urine osmolality and albumin excretion (UAE).]. 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:21834801
;
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:NP786821.RARVwvhwmRsENyE02TorwFoFyCFf4I9YnTRXjvVbX090E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}