@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k
> .
@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 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:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_head
{
this:
np:hasAssertion
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_assertion
;
np:hasProvenance
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_provenance
;
np:hasPublicationInfo
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_assertion
a
np:Assertion
.
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_provenance
a
np:Provenance
.
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNe24ff937df0ee5727faea3d0699e5914
sio:SIO_000628
miriam-gene:348
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_provenance
{
dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_assertion
dct:description
"[Hippocampal but not amygdalar volumes were associated with presence of one or two APOE epsilon4 alleles in MCI and mild AD, while there was no association of APOE epsilon4 allele with rCBF.]. 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:20541374
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}