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http://rdf.disgenet.org/nanopublications.trig#NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8
> .
@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:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_head
{
this:
np:hasAssertion
dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_assertion
;
np:hasProvenance
dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_provenance
;
np:hasPublicationInfo
dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_assertion
a
np:Assertion
.
dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_provenance
a
np:Provenance
.
dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_assertion
{
miriam-gene:1822
a
ncit:C16612
.
lld:C0233794
a
ncit:C7057
.
dgn-gda:DGN4d8a22167a5716b1ddfd34c0fbad144c
sio:SIO_000628
miriam-gene:1822
,
lld:C0233794
;
a
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.
}
dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_provenance
{
dgn-np:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_assertion
dcterms:description
"[In this study, we have established DRPLA transgenic mouse lines (sublines) harboring a single copy of the full-length mutant human DRPLA gene carrying various lengths of expanded CAG repeats (Q76, Q96, Q113, and Q129), which have clearly shown motor deficits and memory disturbance whose severity increases with the length of expanded CAG repeats and age, and successfully replicated the CAG repeat length- and age-dependent features of DRPLA patients.]. 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:22342974
;
prov:wasDerivedFrom
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;
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:NP854777.RAMsPWF8s4713fbyq6whngwWixIpUEpIV67pNLX3s6mV8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:43+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
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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}