@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY
> .
@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:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_head
{
this:
np:hasAssertion
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_assertion
;
np:hasProvenance
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_provenance
;
np:hasPublicationInfo
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_assertion
a
np:Assertion
.
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_provenance
a
np:Provenance
.
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_assertion
{
miriam-gene:5428
a
ncit:C16612
.
lld:C1849096
a
ncit:C7057
.
dgn-gda:DGNcac3b58fcee4f5a80b6387854ba933a4
sio:SIO_000628
miriam-gene:5428
,
lld:C1849096
;
a
sio:SIO_001121
.
}
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_provenance
{
dgn-np:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_assertion
dcterms:description
"[The frequency of the mitochondrial recessive ataxia syndrome (MIRAS) and the infantile onset spinocerebellar ataxia (IOSCA) in this population remains unknown since no case with the common mutation of the corresponding gene was detected.]. 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:18058631
;
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:NP272494.RAJ6hMWK0eOMepl7ZTUhpTR0iekaYuMWdHeXQ8Nad_2zY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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" .
}