@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E
> .
@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:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_head
{
this:
np:hasAssertion
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_assertion
;
np:hasProvenance
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_provenance
;
np:hasPublicationInfo
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_assertion
a
np:Assertion
.
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_provenance
a
np:Provenance
.
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_assertion
{
miriam-gene:114548
a
ncit:C16612
.
lld:C0687720
a
ncit:C7057
.
dgn-gda:DGN390a6a925263f5de3a781a3bbb36e4a8
sio:SIO_000628
miriam-gene:114548
,
lld:C0687720
;
a
sio:SIO_001122
.
}
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_provenance
{
dgn-np:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_assertion
dcterms:description
"[Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) is an inherited disease caused by progressive deficiency of the hormone arginine vasopressin (AVP) that typically becomes clinically apparent in the first decade of life.]. 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:12359138
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47919.RA055qVkpr7FA5xXZQjjoKeS30G1mAoV2cxMuvzYpAD5E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}