@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_head
{
this:
np:hasAssertion
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_assertion
;
np:hasProvenance
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_assertion
a
np:Assertion
.
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_provenance
a
np:Provenance
.
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C0677501
a
ncit:C7057
.
dgn-gda:DGN481bc4ca57ee165cb966cdbb5fd654a2
sio:SIO_000628
miriam-gene:551
,
lld:C0677501
;
a
sio:SIO_001121
.
}
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_provenance
{
dgn-np:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_assertion
dcterms:description
"[To investigate the association of mutations in the arginine vasopressin receptor type II (V2R) gene with congenital nephrogenic diabetes insipidus (CNDI) in the Japanese, we analyzed the V2R gene, located on the X chromosome, in three Japanese pedigrees with CNDI.]. 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:8766937
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1355900.RAcmlxPUQu652bxBW0tpCTAWEoCYb6xAoWFJ3XltORDfA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}