@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY
> .
@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:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_head
{
this:
np:hasAssertion
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_assertion
;
np:hasProvenance
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_provenance
;
np:hasPublicationInfo
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_assertion
a
np:Assertion
.
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_provenance
a
np:Provenance
.
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNc9f68c2fe6fd19ed7a1c34911ddf2616
sio:SIO_000628
miriam-gene:551
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_provenance
{
dgn-np:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_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: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:NP169782.RAYhWjOEpGNHv8eDWx2UVl2Lkmz_5Q49kfGhqygWU3yoY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}