@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8
> .
@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:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_head
{
this:
np:hasAssertion
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_assertion
;
np:hasProvenance
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_provenance
;
np:hasPublicationInfo
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_assertion
a
np:Assertion
.
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_provenance
a
np:Provenance
.
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_assertion
{
miriam-gene:359
a
ncit:C16612
.
lld:C0162283
a
ncit:C7057
.
dgn-gda:DGNde32f1879cfa69a7b8f00932f6289bce
sio:SIO_000628
miriam-gene:359
,
lld:C0162283
;
a
sio:SIO_001121
.
}
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_provenance
{
dgn-np:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_assertion
dcterms:description
"[In this article, we review the current understanding of the known genetic causes of nephrogenic diabetes insipidus that affect the binding of vasopressin to the V2 receptor and subsequent intracellular signaling events, as well as the translocation of aquaporin-2 water channels to the apical membrane.]. 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:14586738
;
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:NP173517.RAWUfAlizz1ngPzjpYR2OfkPGKp_PUyulpMj71aG7L_L8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}