@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_head
{
this:
np:hasAssertion
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_assertion
;
np:hasProvenance
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_provenance
;
np:hasPublicationInfo
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_assertion
a
np:Assertion
.
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_provenance
a
np:Provenance
.
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNad7094d76c4025c5e4abc132dd357b09
sio:SIO_000628
miriam-gene:351
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_provenance
{
dgn-np:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_assertion
dcterms:description
"[Our results suggest that APP mutations in the Aβ coding region favour Aβ38 accumulation in the brain and that the molecular mechanisms of Aβ deposition in these patients may be different from those active in patients with familial AD associated with other genetic defects and sporadic AD.]. 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:23143229
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1027531.RAfUEk85w6a1Gi-gIOKhhhJ1BOTyDD_OIeUQgeOgaGwic130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:31+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}