@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_head
{
this:
np:hasAssertion
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_assertion
;
np:hasProvenance
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_provenance
;
np:hasPublicationInfo
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_assertion
a
np:Assertion
.
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_provenance
a
np:Provenance
.
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNd76b00df2d1a154de4de50dd9a193801
sio:SIO_000628
miriam-gene:348
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_provenance
{
dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_assertion
dcterms:description
"[Results confirmed that APOE 4 allele associated with increased NFT stages and cognitive decline, with carriers with one APOE ε2 or ε3 allele often having better clinical outcomes compared to carriers with none or two ε2 or ε3 alleles respectively.]. 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:21605063
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:30+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}