@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A
> .
@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:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_head
{
this:
np:hasAssertion
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_assertion
;
np:hasProvenance
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_provenance
;
np:hasPublicationInfo
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_assertion
a
np:Assertion
.
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_provenance
a
np:Provenance
.
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_assertion
{
miriam-gene:114548
a
ncit:C16612
.
lld:C0162283
a
ncit:C7057
.
dgn-gda:DGN5c31102b01f7502dabca59fb1bb9c6b2
sio:SIO_000628
miriam-gene:114548
,
lld:C0162283
;
a
sio:SIO_001121
.
}
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_provenance
{
dgn-np:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_assertion
dcterms:description
"[The essential role of the vasopressin V2 receptor and AQP2 in the maintenance of body water homeostasis became clear when it was shown that mutations in their genes cause nephrogenic diabetes insipidus, a disorder in which the kidney is unable to concentrate urine in response to AVP.]. 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:18519086
;
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:NP181177.RAi7woaYXVwkVh9XkAQ_2aVPNwn1N70iz89Tkzrgh5h_A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}