@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4
> .
@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:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_head
{
this:
np:hasAssertion
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_assertion
;
np:hasProvenance
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_provenance
;
np:hasPublicationInfo
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_assertion
a
np:Assertion
.
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_provenance
a
np:Provenance
.
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_assertion
{
miriam-gene:492
a
ncit:C16612
.
lld:C0007758
a
ncit:C7057
.
dgn-gda:DGN9821d3b2fd37490091aed2bbf52a186d
sio:SIO_000628
miriam-gene:492
,
lld:C0007758
;
a
sio:SIO_001121
.
}
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_provenance
{
dgn-np:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_assertion
dcterms:description
"[Olivopontocerebellar atrophy with retinal degeneration (OPCA type III) and autosomal dominant cerebellar atrophy of late onset (type II) appear to represent the same disease which is characterized by dominantly inherited cerebellar ataxia and pigmentary retinal degeneration.]. 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:8233354
;
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:NP319948.RAOwJ99PU7zK34Gj4pn4QbLPRuxeeccONZl2qKrAxCPg4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}