@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I
> .
@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:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_head
{
this:
np:hasAssertion
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_assertion
;
np:hasProvenance
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_provenance
;
np:hasPublicationInfo
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_assertion
a
np:Assertion
.
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_provenance
a
np:Provenance
.
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_assertion
{
miriam-gene:9333
a
ncit:C16612
.
lld:C0018790
a
ncit:C7057
.
dgn-gda:DGNd7589475b18487b2bd22257545e49169
sio:SIO_000628
miriam-gene:9333
,
lld:C0018790
;
a
sio:SIO_001122
.
}
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_provenance
{
dgn-np:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_assertion
dcterms:description
"[Mutations in TGM6 were ascertained in 109 unrelated probands of Chinese descent with molecularly unassigned SCA from 512 pedigrees, in whom mutations responsible for 15 other ataxia syndromes had been excluded.]. 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:25253745
;
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:NP820343.RAcvYKYjQVVbOqCNcVU-OKzNXytDibxaMb6hU-i36XS7I130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:57+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" .
}