@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c
> .
@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:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_head
{
this:
np:hasAssertion
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_assertion
;
np:hasProvenance
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_provenance
;
np:hasPublicationInfo
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_assertion
a
np:Assertion
.
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_provenance
a
np:Provenance
.
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0026650
a
ncit:C7057
.
dgn-gda:DGN97c491ae2c958e7851e91aaca8872d2d
sio:SIO_000628
miriam-gene:1861
,
lld:C0026650
;
a
sio:SIO_001121
.
}
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_provenance
{
dgn-np:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_assertion
dcterms:description
"[High resolution melting (HRM) was used to examine the entire TOR1A Exon 5 coding sequence in 1014 subjects with primary dystonia (422 spasmodic dysphonia, 285 cervical dystonia, 67 blepharospasm, 41 writer's cramp, 16 oromandibular dystonia, 38 other primary focal dystonia, 112 segmental dystonia, 16 multifocal dystonia, and 17 generalized dystonia) and 250 controls (150 neurologically normal and 100 with other movement disorders).]. 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:19284587
;
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:NP356703.RATN7kkZaKMx0QNgJ5ew2tbo4p2u3Hm5aZalXVSDBOO6c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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" .
}