@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY
> .
@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:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_head
{
this:
np:hasAssertion
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_assertion
;
np:hasProvenance
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_provenance
;
np:hasPublicationInfo
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_assertion
a
np:Assertion
.
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_provenance
a
np:Provenance
.
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_assertion
{
miriam-gene:359
a
ncit:C16612
.
lld:C3714756
a
ncit:C7057
.
dgn-gda:DGNb15d020f2166b1a12df3ddca7820ebc2
sio:SIO_000628
miriam-gene:359
,
lld:C3714756
;
a
sio:SIO_001122
.
}
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_provenance
{
dgn-np:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_assertion
dcterms:description
"[AQP2 mutation in NDI families and perinatal mutation testing is of direct clinical value because early diagnosis and treatment can avert the physical and mental retardation associated with repeated episodes of dehydration.]. 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:16580609
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP216398.RAnYQxe3cb_Vyg91KYIZn9Q2KMGeqFCQAXO3AH_m3HSrY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:24+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" .
}