@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho
> .
@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:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_head
{
this:
np:hasAssertion
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_assertion
;
np:hasProvenance
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_provenance
;
np:hasPublicationInfo
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_assertion
a
np:Assertion
.
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_provenance
a
np:Provenance
.
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C0011175
a
ncit:C7057
.
dgn-gda:DGN732e363ca9a95e3eefcc59292fdf81e0
sio:SIO_000628
miriam-gene:551
,
lld:C0011175
;
a
sio:SIO_001121
.
}
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_provenance
{
dgn-np:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_assertion
dcterms:description
"[We have proposed that all families with hereditary diabetes insipidus should have their molecular defect identified because early diagnosis and treatment of affected infants can avert the physical and mental retardation that results from repeated episodes of dehydration.]. 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:18519085
;
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:NP707451.RA8IlPuA2jlXmHNkybb2hiXrUJRn14tX82lKwttk3Yvho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}