@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I
> .
@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:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_head
{
this:
np:hasAssertion
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_assertion
;
np:hasProvenance
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_provenance
;
np:hasPublicationInfo
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_assertion
a
np:Assertion
.
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_provenance
a
np:Provenance
.
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_assertion
{
miriam-gene:5294
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNf69a630b7b27c61dafd894895ab3e990
sio:SIO_000628
miriam-gene:5294
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_provenance
{
dgn-np:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_assertion
dcterms:description
"[While the PI3K/Akt pathway has been shown to regulate multiple cellular events pertinent to AD pathogenesis, potential functions of tumor suppressor phosphatase and tensin homologue deleted on chromosome 10 (PTEN) in AD pathogenesis have not been explored.]. 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:16645045
;
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:NP821427.RAGGhDyEwEcHHodjbbHj7Rnr3FI7TM86lZSwtyVk8ZN5I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}