@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0
> .
@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:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_head
{
this:
np:hasAssertion
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_assertion
;
np:hasProvenance
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_provenance
;
np:hasPublicationInfo
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_assertion
a
np:Assertion
.
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_provenance
a
np:Provenance
.
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0751781
a
ncit:C7057
.
dgn-gda:DGN6bd56780a9625f60bef63a4aa41a4075
sio:SIO_000628
miriam-gene:367
,
lld:C0751781
;
a
sio:SIO_001121
.
}
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_provenance
{
dgn-np:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_assertion
dcterms:description
"[5), Huntington's disease (69.0) and spinal and bulbar muscular atrophy (16.3), which is consistent with the clinical observation that the genetic anticipation on the paternal transmission of DRPLA is the most prominent among CAG repeat diseases.]. 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:9949204
;
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:NP411396.RAmCww97zTZXcZ0AtQU1i0xoIi41mMx6ulN-GVGdmGST0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}