@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs
> .
@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:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_head
{
this:
np:hasAssertion
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_assertion
;
np:hasProvenance
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_provenance
;
np:hasPublicationInfo
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_assertion
a
np:Assertion
.
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_provenance
a
np:Provenance
.
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGNb1f1307e41cef70593ac7ea7e524313e
sio:SIO_000628
miriam-gene:3064
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_provenance
{
dgn-np:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_assertion
dcterms:description
"[Because analysis of the Huntingtin gene revealed normal alleles and various of the patients had seizures, we analysed the B37 gene and found significantly elongated CAG repeats as have been reported in DRPLA.]. 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:7868125
;
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:NP837042.RAPenhMGAj59UpMP6dm79owpqjccx-mLls2-9-B5eHSfs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:32+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" .
}