@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go
> .
@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:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_head
{
this:
np:hasAssertion
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_assertion
;
np:hasProvenance
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_provenance
;
np:hasPublicationInfo
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_assertion
a
np:Assertion
.
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_provenance
a
np:Provenance
.
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_assertion
{
miriam-gene:7314
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGN3460ae60c899307c26571a3ff99646ca
sio:SIO_000628
miriam-gene:7314
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_provenance
{
dgn-np:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_assertion
dcterms:description
"[UBB+1 accumulates in the neuritic plaques and neurofibrillary tangles in all patients with AD (Alzheimer's disease) and in the neuronal and glial hallmarks of other tauopathies and in polyglutamine diseases such as Huntington's disease.]. 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:17052186
;
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:NP603601.RAm4bm63PnD9gf1Rs1dV6mPgy1qSoxndZxEwvxlcDk2Go130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:02+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" .
}