@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M
> .
@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:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_head
{
this:
np:hasAssertion
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_assertion
;
np:hasProvenance
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_provenance
;
np:hasPublicationInfo
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_assertion
a
np:Assertion
.
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_provenance
a
np:Provenance
.
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNc533e4abf1d90f1544657afc1e13cab7
sio:SIO_000628
miriam-gene:551
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_provenance
{
dgn-np:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_assertion
dcterms:description
"[Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) is an inherited disease caused by progressive degeneration of the magnocellular neurons of the hypothalamus leading to decreased ability to produce the hormone arginine vasopressin (AVP).]. 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:9360520
;
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:NP741531.RAV6Nu3arAXW2x27vu9JE_EQye6t9TXr7hoQ8mbZqBV2M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}