@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs
> .
@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:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_head
{
this:
np:hasAssertion
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_assertion
;
np:hasProvenance
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_provenance
;
np:hasPublicationInfo
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_assertion
a
np:Assertion
.
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_provenance
a
np:Provenance
.
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C0041341
a
ncit:C7057
.
dgn-gda:DGN7dcdfa7780b193554f1f2897f7cc0085
sio:SIO_000628
miriam-gene:5290
,
lld:C0041341
;
a
sio:SIO_001121
.
}
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_provenance
{
dgn-np:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_assertion
dcterms:description
"[The collective data discussed have laid the groundwork for important new insights into the many cancers caused by aberrant PI3K activation and the clinically challenging tuberous sclerosis complex disease and have suggested a possible means of treatment for both.]. 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:12773158
;
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:NP262508.RA08xEcxcwb4cZvlZS1aMIdvQ4zV9ykM2WRlSQNtyVbxs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}