@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo
> .
@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:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_head
{
this:
np:hasAssertion
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_assertion
;
np:hasProvenance
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_provenance
;
np:hasPublicationInfo
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_assertion
a
np:Assertion
.
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_provenance
a
np:Provenance
.
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_assertion
{
miriam-gene:554
a
ncit:C16612
.
lld:C0162283
a
ncit:C7057
.
dgn-gda:DGN635997eb00802e48c6c02ecf3acaa1db
sio:SIO_000628
miriam-gene:554
,
lld:C0162283
;
a
sio:SIO_001121
.
}
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_provenance
{
dgn-np:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_assertion
dcterms:description
"[X-linked recessive nephrogenic diabetes insipidus is caused by mutations in the gene encoding the V2 vasopressin receptor (V2R), the mediator of the antidiuretic effect of arginine vasopressin (AVP) in mammalian kidneys.]. 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:10714359
;
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:NP218929.RASW2gGePgkY0eOMrgQB_vMkJ8B4cHuKXobMVOTuIEzqo130_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" .
}