@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo
> .
@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:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_head
{
this:
np:hasAssertion
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_assertion
;
np:hasProvenance
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_provenance
;
np:hasPublicationInfo
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_assertion
a
np:Assertion
.
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_provenance
a
np:Provenance
.
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_assertion
{
miriam-gene:759
a
ncit:C16612
.
lld:C0333463
a
ncit:C7057
.
dgn-gda:DGNa8283b8e13f0c91c012fe9a3bfdfa12f
sio:SIO_000628
miriam-gene:759
,
lld:C0333463
;
a
sio:SIO_001121
.
}
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_provenance
{
dgn-np:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_assertion
dcterms:description
"[Neuropathology shows diffuse cerebral atrophy with neurofibrillary tangles, often ghost tangles, and neuropil threads almost limited to limbic areas (transentorhinal, entorhinal area, hippocampuS--not exclusively sector CA 1--and amygdala) with only rare and mild involvement of the neocortex, basal ganglia and brainstem (except nucleus basalis and locus ceruleus), absence of neuritic plaques and absence or scarcety of amyloid deposits.]. 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:9546293
;
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:NP752761.RAIDIDL-E4yj69DyAbOurEmKetLX8TDBMDUuvFf19UUxo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}