@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY
> .
@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:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_head
{
this:
np:hasAssertion
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_assertion
;
np:hasProvenance
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_assertion
a
np:Assertion
.
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_provenance
a
np:Provenance
.
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C1842937
a
ncit:C7057
.
dgn-gda:DGN7f3a7eb9e6b74b528e827f94bb7f6095
sio:SIO_000628
miriam-gene:351
,
lld:C1842937
;
a
sio:SIO_001121
.
}
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_provenance
{
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_assertion
dcterms:description
"[Although several factors may contribute to CAA in humans, the neuronal origin of transgenic APP, high levels of Abeta in cerebrospinal fluid, and regional localization of CAA in APP23 mice suggest transport and drainage pathways rather than local production or blood uptake of Abeta as a primary mechanism underlying cerebrovascular amyloid 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:10570203
;
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:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}