@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI
> .
@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:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_head
{
this:
np:hasAssertion
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_assertion
;
np:hasProvenance
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_provenance
;
np:hasPublicationInfo
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_assertion
a
np:Assertion
.
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_provenance
a
np:Provenance
.
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C0020488
a
ncit:C7057
.
dgn-gda:DGNceffc95431597078b85d2e29f21600ed
sio:SIO_000628
miriam-gene:5443
,
lld:C0020488
;
a
sio:SIO_001121
.
}
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_provenance
{
dgn-np:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_assertion
dcterms:description
"[These results suggest that adNDI is a progressive disease associated with chronic loss of the magnocellular neurons that supply AVP to the posterior pituitary but preservation of the parvocellular neurons that supply AVP and CRH to the median eminence and stimulate ACTH production during hypernatremia.]. 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:11836335
;
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:NP412788.RAEnKIkH8VVJlnGRyt9ETlqb_CFLf16ry9wQMjW03bmDI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}