@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg
> .
@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:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_head
{
this:
np:hasAssertion
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_assertion
;
np:hasProvenance
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_provenance
;
np:hasPublicationInfo
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_assertion
a
np:Assertion
.
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_provenance
a
np:Provenance
.
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_assertion
{
miriam-gene:3454
a
ncit:C16612
.
lld:C0011848
a
ncit:C7057
.
dgn-gda:DGNcd747bdd1c387fdb4e97be4cb92db8f6
sio:SIO_000628
miriam-gene:3454
,
lld:C0011848
;
a
sio:SIO_001121
.
}
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_provenance
{
dgn-np:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_assertion
dcterms:description
"[Diabetes insipidus represents a dramatic but rare disturbance of water balance caused by deficient AVP secretion (neurogenic), reduced renal sensitivity to AVP (nephrogenic), an abnormally high fluid intake (primary polydipsia), or in rare cases by placental enzymatic degradation of AVP (gestational).]. 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:17727573
;
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:NP366476.RANNoxJjo-v-r-mN9NyLQzEUbqTTUpU9hvLJX-IJN2SJg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:34+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" .
}