@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o
> .
@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:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_head
{
this:
np:hasAssertion
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_assertion
;
np:hasProvenance
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_assertion
a
np:Assertion
.
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_provenance
a
np:Provenance
.
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_assertion
{
miriam-gene:30833
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN16e4847200975b3453d2b05605cdbfd3
sio:SIO_000628
miriam-gene:30833
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_provenance
{
dgn-np:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_assertion
dcterms:description
"[These findings indicate that in DRPLA, the NIFIs in the CDN are an alteration that is directly related to the causative gene abnormality (an expanded CAG repeat encoding polyglutamine) and that, from the molecular point of view, they are distinct from the SLIs in ALS.]. 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:10867794
;
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:NP806598.RA6z6Vxu_frPN46o83s0ZzkoJ251Nnp_m3B98lgfZ6S1o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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: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" .
}