@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_head
{
this:
np:hasAssertion
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_assertion
;
np:hasProvenance
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_provenance
;
np:hasPublicationInfo
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_assertion
a
np:Assertion
.
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_provenance
a
np:Provenance
.
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_assertion
{
miriam-gene:23064
a
ncit:C16612
.
lld:C0013421
a
ncit:C7057
.
dgn-gda:DGN452d1ed93607b2001b1b8fb579793eba
sio:SIO_000628
miriam-gene:23064
,
lld:C0013421
;
a
sio:SIO_001121
.
}
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_provenance
{
dgn-np:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_assertion
dcterms:description
"[Pyramidal signs and dystonia were more frequent and disease was less severe with missense mutations in the helicase domain of senataxin gene than with missense mutations out of helicase domain and deletion and nonsense mutations (P = 0.001, P = 0.008 and P = 0.01, respectively).]. 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:19696032
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP867791.RAiGJwM-F9cU93b0GXkA2DSeqT-AwqZLb4sOnBOky4IAM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:27+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}