@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98
> .
@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:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_head
{
this:
np:hasAssertion
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_assertion
;
np:hasProvenance
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_provenance
;
np:hasPublicationInfo
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_assertion
a
np:Assertion
.
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_provenance
a
np:Provenance
.
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGN9b4aa95b0b77c227f089245c56a61132
sio:SIO_000628
miriam-gene:3918
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_provenance
{
dgn-np:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_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:NP659139.RAA8oHLpGVPSIsHTLyWIORpRYntf-VSCYbBTXfM3C9a98130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:38+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" .
}