@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k
> .
@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:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_head
{
this:
np:hasAssertion
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_assertion
;
np:hasProvenance
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_provenance
;
np:hasPublicationInfo
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_assertion
a
np:Assertion
.
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_provenance
a
np:Provenance
.
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNa3e78e3c508170bf07e07ea76880cfc6
sio:SIO_000628
miriam-gene:7276
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_provenance
{
dgn-np:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_assertion
dcterms:description
"[Supporting this view are the reduced TTR levels found in CSF of patients with AD, as well as reports of altered TTR expression in the cortex and hippocampus of AD rodent models.]. 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:16698124
;
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:NP917783.RA1hPKgv9-kRpHohw_f9iCprQWrBuHPCUQc0-sL20Pe6k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}