@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM
> .
@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:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_head
{
this:
np:hasAssertion
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_assertion
;
np:hasProvenance
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_provenance
;
np:hasPublicationInfo
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_assertion
a
np:Assertion
.
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_provenance
a
np:Provenance
.
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0002622
a
ncit:C7057
.
dgn-gda:DGN5960a2bf05e2e8524f9d74690092eb61
sio:SIO_000628
miriam-gene:348
,
lld:C0002622
;
a
sio:SIO_001121
.
}
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_provenance
{
dgn-np:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_assertion
dcterms:description
"[To determine whether memory loss is detectable before the symptomatic presentation of mild cognitive impairment (MCI) in those at greater genetic risk for Alzheimer disease (AD) based upon presence or absence of the e4 allele of APOE.]. 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:15184602
;
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:NP807323.RA1-UOUY65OX-mz7ARnbEOoLSvwICx0u-X5JOgnMgYuXM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:15+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" .
}