@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU
> .
@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:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_head
{
this:
np:hasAssertion
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_assertion
;
np:hasProvenance
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_provenance
;
np:hasPublicationInfo
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_assertion
a
np:Assertion
.
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_provenance
a
np:Provenance
.
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_assertion
{
miriam-gene:6311
a
ncit:C16612
.
lld:C0038868
a
ncit:C7057
.
dgn-gda:DGN3ec52dbe832690751a6bce4b140a4047
sio:SIO_000628
miriam-gene:6311
,
lld:C0038868
;
a
sio:SIO_001121
.
}
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_provenance
{
dgn-np:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_assertion
dcterms:description
"[In conclusion, our findings confirm the role of ATXN2 as an important risk factor for ALS and support the hypothesis that expanded ATXN2 repeats may predispose to other neurodegenerative diseases, including progressive supranuclear palsy.]. 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:21610160
;
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:NP896598.RA4PitbkCA7T3NpeU3-judIN8i3UkooViqx5pyTy83hmU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:30+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: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" .
}