@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8
> .
@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:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_head
{
this:
np:hasAssertion
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_assertion
;
np:hasProvenance
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_provenance
;
np:hasPublicationInfo
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_assertion
a
np:Assertion
.
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_provenance
a
np:Provenance
.
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0020256
a
ncit:C7057
.
dgn-gda:DGN5cf97f130688d312c1c02698ecb667f1
sio:SIO_000628
miriam-gene:3918
,
lld:C0020256
;
a
sio:SIO_001121
.
}
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_provenance
{
dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_assertion
dcterms:description
"[Here we show that conditional inactivation of the Hdh gene in Wnt1 cell lineages results in congenital hydrocephalus, implicating huntingtin for the first time in the regulation of cerebral spinal fluid (CSF) homeostasis.]. 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:18838463
;
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:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:51+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" .
}