@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4
> .
@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:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_head
{
this:
np:hasAssertion
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_assertion
;
np:hasProvenance
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_provenance
;
np:hasPublicationInfo
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_assertion
a
np:Assertion
.
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_provenance
a
np:Provenance
.
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0752353
a
ncit:C7057
.
dgn-gda:DGN2bd97bb28da3d166ca8ce2f99cd6ef7a
sio:SIO_000628
miriam-gene:3064
,
lld:C0752353
;
a
sio:SIO_001121
.
}
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_provenance
{
dgn-np:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_assertion
dcterms:description
"[Spinobulbar muscular atrophy and Huntington's disease are caused by polyglutamine expansion in the androgen receptor and huntingtin, respectively, and their pathogenesis has been associated with abnormal nuclear localization and aggregation of truncated forms of these proteins.]. 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:10639135
;
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:NP906138.RA0_lNcvhT4nkK4qgbzyA0vrMNU8CkCAX0HQW2uxsiIO4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:16+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" .
}