@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0
> .
@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:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_head
{
this:
np:hasAssertion
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_assertion
;
np:hasProvenance
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_provenance
;
np:hasPublicationInfo
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_assertion
a
np:Assertion
.
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_provenance
a
np:Provenance
.
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C2931784
a
ncit:C7057
.
dgn-gda:DGNa73dfb9171a84eabf9c500164804d0f7
sio:SIO_000628
miriam-gene:1437
,
lld:C2931784
;
a
sio:SIO_001121
.
}
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_provenance
{
dgn-np:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_assertion
dcterms:description
"[The defective clearance of amyloid leads to amyloid angiopathy that in turn perpetuates hypoperfusion that affects formation as well as absorption of CSF thereby altering clearance of amyloid and promoting vascular and parenchymal deposition[1].]. 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:16611010
;
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:NP780900.RATfI3vuVKQtFX3zij22cXztyR9ldl9L02n1jtZHD4nz0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}