@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA
> .
@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:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_head
{
this:
np:hasAssertion
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_assertion
;
np:hasProvenance
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_provenance
;
np:hasPublicationInfo
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_assertion
a
np:Assertion
.
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_provenance
a
np:Provenance
.
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN202b60a1833570efae3c4a555de9cd23
sio:SIO_000628
miriam-gene:5290
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_provenance
{
dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_assertion
dcterms:description
"[The phosphoinositide 3-kinase (PI3K)/Akt pathway has been implicated in the pathogenesis of AD, however, potential functions and role of tumor suppressor phosphatase and tensin homologue deleted on chromosome 10 (PTEN) in AD pathogenesis have not been fully 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:22906543
;
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:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}