@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs
> .
@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:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_head
{
this:
np:hasAssertion
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_assertion
;
np:hasProvenance
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_provenance
;
np:hasPublicationInfo
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_assertion
a
np:Assertion
.
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_provenance
a
np:Provenance
.
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGN9cf528b9fa1320fd64ae5ec3245f27d9
sio:SIO_000628
miriam-gene:1437
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_provenance
{
dgn-np:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_assertion
dcterms:description
"[Neuropathological studies of young deceased ε4 carriers have shown modest but abnormal amounts of neocortical amyloid and medial temporal neurofibrillary tangles that is also reflected in cerebrospinal fluid (CSF) biomarkers, amyloid-β, and phospho-tau in particular.]. 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:22695623
;
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:NP608936.RAfnHyYSUeSFExTOyOauXk6UI2OaQeqzqrynaeuVCfBgs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}