@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M
> .
@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:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_head
{
this:
np:hasAssertion
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_assertion
;
np:hasProvenance
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_provenance
;
np:hasPublicationInfo
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_assertion
a
np:Assertion
.
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_provenance
a
np:Provenance
.
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_assertion
{
miriam-gene:1270
a
ncit:C16612
.
lld:C0525041
a
ncit:C7057
.
dgn-gda:DGN6f51689c0d986b36ecd81b868670e84b
sio:SIO_000628
miriam-gene:1270
,
lld:C0525041
;
a
sio:SIO_001121
.
}
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_provenance
{
dgn-np:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_assertion
dcterms:description
"[These results support the hypothesis that CNTF infusion into the striatum of HD patients not only could block the degeneration of neurons but also alleviated motor and cognitive symptoms associated with persistent neuronal dysfunction.]. 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:10834619
;
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:NP782882.RAdEGjqkoKkRsL_Fj4-KGyWVfuFk_IXLk-L2VhKRvg6-M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}