@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A
> .
@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/v4.0.0/void/
> .
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_head
{
this:
np:hasAssertion
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_assertion
;
np:hasProvenance
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_provenance
;
np:hasPublicationInfo
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_assertion
a
np:Assertion
.
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_provenance
a
np:Provenance
.
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_assertion
{
miriam-gene:343641
a
ncit:C16612
.
lld:C0018790
a
ncit:C7057
.
dgn-gda:DGNb545ef17378da6eaea518e3ec1157a11
sio:SIO_000628
miriam-gene:343641
,
lld:C0018790
;
a
sio:SIO_001122
.
}
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_provenance
{
dgn-np:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1223405.RAdc568kDhrEXwb690QGLdtrh73ClRVxQtt3soFJe9q7A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:00+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}