@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8
> .
@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:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_head
{
this:
np:hasAssertion
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_assertion
;
np:hasProvenance
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_provenance
;
np:hasPublicationInfo
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_assertion
a
np:Assertion
.
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_provenance
a
np:Provenance
.
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGN1f7e4222a77f3ff5df59ebdc8119c09f
sio:SIO_000628
miriam-gene:367
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_provenance
{
dgn-np:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_assertion
dcterms:description
"[Subsequent to the identification of the mutation in SBMA, other inherited neurodegenerative diseases have been found to be caused by the expansion of CAG repeats in the coding regions of other genes.]. 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:8545913
;
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:NP336728.RAOtwIeaBu5oc4Sf_zPtrmKjo4tB269o09WOdzHw1gfG8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:18+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" .
}