@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA
> .
@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:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_head
{
this:
np:hasAssertion
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_assertion
;
np:hasProvenance
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_provenance
;
np:hasPublicationInfo
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_assertion
a
np:Assertion
.
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_provenance
a
np:Provenance
.
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0750901
a
ncit:C7057
.
dgn-gda:DGN341c2cc71f22083a83b403b5a8abe98c
sio:SIO_000628
miriam-gene:351
,
lld:C0750901
;
a
sio:SIO_001121
.
}
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_provenance
{
dgn-np:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_assertion
dcterms:description
"[These findings strongly implicate APP and the betaCTF of APP, and exclude Abeta and the alphaCTF, as the cause of endocytic pathway dysfunction in DS and AD, underscoring the potential multifaceted value of BACE-1 inhibition in AD therapeutics.]. 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:20080541
;
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:NP325823.RAPeJyikXqr0leN0xFIm7HOezNbdCqYmP9iE7yGlYtCqA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}