@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ
> .
@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:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_head
{
this:
np:hasAssertion
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_assertion
;
np:hasProvenance
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_assertion
a
np:Assertion
.
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_provenance
a
np:Provenance
.
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_assertion
{
miriam-gene:3454
a
ncit:C16612
.
lld:C0687720
a
ncit:C7057
.
dgn-gda:DGNd2a32f0b70d9033b16621d3c3432b51c
sio:SIO_000628
miriam-gene:3454
,
lld:C0687720
;
a
sio:SIO_001121
.
}
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_provenance
{
dgn-np:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_assertion
dcterms:description
"[X-linked nephrogenic diabetes insipidus (XNDI), caused by mutations in the V2 vasopressin receptor (V2R), is clinically distinguished from central diabetes insipidus (CDI) by elevated serum vasopressin (AVP) levels and unresponsiveness to 1-desamino-8-d-arginine vasopressin (DDAVP).]. 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:19170711
;
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:NP219189.RA-VcbI8RGdqzi2ME2Cz57nDbNIWqwNsUcZsPzkZmEGdQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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" .
}