@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY
> .
@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:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_head
{
this:
np:hasAssertion
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_assertion
;
np:hasProvenance
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_provenance
;
np:hasPublicationInfo
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_assertion
a
np:Assertion
.
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_provenance
a
np:Provenance
.
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_assertion
{
miriam-gene:6712
a
ncit:C16612
.
lld:C0037952
a
ncit:C7057
.
dgn-gda:DGN43af72e2246cd7d2ac1e892d79ea2cbc
sio:SIO_000628
miriam-gene:6712
,
lld:C0037952
;
a
sio:SIO_001121
.
}
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_provenance
{
dgn-np:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_assertion
dcterms:description
"[This widespread degeneration pattern goes clearly beyond purely cerebellar degenerations such as SCA5 and 6 and beyond spinocerebellar degenerations such as SCA1, 3, 7, also involves regions known to degenerate in Huntington's disease, and is quite similar to the degeneration pattern in sporadic patients with multi-system atrophy.]. 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:10090679
;
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:NP743297.RA2R3XoB21xQZPfYkTM1_pax9AsNYYnYmYUPieJ8PM4eY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}