@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_head
{
this:
np:hasAssertion
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_assertion
;
np:hasProvenance
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_provenance
;
np:hasPublicationInfo
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_assertion
a
np:Assertion
.
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_provenance
a
np:Provenance
.
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN654c6c6d64079d44e1d807be40fa27ce
sio:SIO_000628
miriam-gene:3064
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_provenance
{
dgn-np:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_assertion
dcterms:description
"[Use of RNA interference to reduce huntingtin protein (htt) expression in affected brain regions may provide an effective treatment for Huntington disease (HD), but it remains uncertain whether suppression of both wild-type and mutant alleles in a heterozygous patient will provide more benefit than harm.]. 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:19289118
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP726365.RAO1Clu867vQCimOGqEoJs0cLkbr6tF29yUOqKBlF1HB4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:14+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}