@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc
> .
@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:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_head
{
this:
np:hasAssertion
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_assertion
;
np:hasProvenance
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_provenance
;
np:hasPublicationInfo
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_assertion
a
np:Assertion
.
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_provenance
a
np:Provenance
.
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_assertion
{
miriam-gene:5524
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNb45d0e9cd3a5d5107df8aa1fadc98faf
sio:SIO_000628
miriam-gene:5524
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_provenance
{
dgn-np:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_assertion
dcterms:description
"[Taken together, these findings suggest that increased PP2A phosphorylation (Y307) can be mediated by Abeta deposition or oestrogen deficiency in the AD brain, and consequently compromise dephosphorylation of abnormally hyperphosphorylated tau, and lead to neurofibrillary tangle formation.]. 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:18208556
;
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:NP599935.RACQHGegLcc7_fU0vMpY_oyLEB-D6-UEM71tTEru6e-Zc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}