@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA
> .
@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 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:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_head
{
this:
np:hasAssertion
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion
;
np:hasProvenance
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_provenance
;
np:hasPublicationInfo
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion
a
np:Assertion
.
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_provenance
a
np:Provenance
.
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion
{
miriam-gene:4287
a
ncit:C16612
.
lld:C0035258
a
ncit:C7057
.
dgn-gda:DGN4c3e319f6ba440e3f33963665f696af5
sio:SIO_000628
miriam-gene:4287
,
lld:C0035258
;
a
sio:SIO_001122
.
}
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_provenance
{
dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion
dct:description
"[To evaluate the contribution of SCA alleles to idiopathic RLS we investigated the CAG repeat length at the SCA1, SCA2, SCA3, SCA6, SCA7, and SCA17 loci in 215 patients who fulfilled the clinical criteria of RLS and presented periodic leg movements in sleep (PLMS) in polysomnographic recording.]. 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:16389595
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}