@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE
> .
@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:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_head
{
this:
np:hasAssertion
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_assertion
;
np:hasProvenance
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_provenance
;
np:hasPublicationInfo
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_assertion
a
np:Assertion
.
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_provenance
a
np:Provenance
.
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_assertion
{
miriam-gene:5521
a
ncit:C16612
.
lld:C0087012
a
ncit:C7057
.
dgn-gda:DGN0f80a3c2f5e745dd05f397febcee67b1
sio:SIO_000628
miriam-gene:5521
,
lld:C0087012
;
a
sio:SIO_001121
.
}
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_provenance
{
dgn-np:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_assertion
dcterms:description
"[Results suggest that Parkinsonism (PD) and multiple system atrophy (MSA) are not associated with spinocerebellar ataxia 12 (SCA12) and it is not necessary to screen SCA12 in PD and MSA 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:18973067
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP110262.RASoZVxpG-W7FJSxFRj2R8esPKOlxljCmOBkw0P13m9oE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:56+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" .
}