@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE
> .
@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:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_head
{
this:
np:hasAssertion
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_assertion
;
np:hasProvenance
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_provenance
;
np:hasPublicationInfo
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_assertion
a
np:Assertion
.
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_provenance
a
np:Provenance
.
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN5a57e02a93618b6b4e991f42daa7d37b
sio:SIO_000628
miriam-gene:351
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_provenance
{
dgn-np:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_assertion
dcterms:description
"[These results suggest that the phosphorylation of APP intracellular domain (AICD) at T668 contributes to the neuronal degeneration in Alzheimer's disease (AD) by regulating its translocation into the nucleus and then affects neurodegeneration.]. 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:16705182
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP110782.RADR4uMeEqlu6yjyP6RTxvPK576Iu0_Fxsp8RWR4y97tE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:56+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" .
}