@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4
> .
@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:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_head
{
this:
np:hasAssertion
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_assertion
;
np:hasProvenance
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_provenance
;
np:hasPublicationInfo
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_assertion
a
np:Assertion
.
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_provenance
a
np:Provenance
.
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN5c16f2f7f47de4f5926e9d2392b9b484
sio:SIO_000628
miriam-gene:1437
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_provenance
{
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_assertion
dcterms:description
"[This was in contrast to the PSEN1 and APPswe mutation carriers revealing high PiB retention in the cortex and the striatum in combination with abnormal glucose metabolism and CSF biomarkers, and the patients with sAD who showed typically high cortical PiB retention and pathologic CSF levels as well as decreased glucose metabolism when compared with HCs.]. 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:22700814
;
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:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}