@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU
> .
@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:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_head
{
this:
np:hasAssertion
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_assertion
;
np:hasProvenance
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_provenance
;
np:hasPublicationInfo
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_assertion
a
np:Assertion
.
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_provenance
a
np:Provenance
.
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGN77844d56d5696e15220611c1266b1505
sio:SIO_000628
miriam-gene:348
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_provenance
{
dgn-np:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_assertion
dcterms:description
"[However, the association studies revealed a significant genetic interaction between the APOE ε4 allele and SIGMAR1 2P carriers in both populations, i.e., in APOE non ε4 allele carriers, SIGMAR1 2P variant had increased cognitive dysfunction and more advanced stages of NFT.]. 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:NP896154.RAP5v78Ex3WIVgfK5jheOonI6d401Ir6A1MFIWObEn8aU130_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" .
}