@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI
> .
@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:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_head
{
this:
np:hasAssertion
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_assertion
;
np:hasProvenance
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_provenance
;
np:hasPublicationInfo
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_assertion
a
np:Assertion
.
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_provenance
a
np:Provenance
.
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_assertion
{
miriam-gene:9628
a
ncit:C16612
.
lld:C0041341
a
ncit:C7057
.
dgn-gda:DGN1da0d8bbeb3bde93f41baef9f90928cd
sio:SIO_000628
miriam-gene:9628
,
lld:C0041341
;
a
sio:SIO_001121
.
}
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_provenance
{
dgn-np:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_assertion
dcterms:description
"[The complex of AS250 with KIAA1219 is notably similar to the important regulatory complex of the protein tuberin with hamartin (the tuberous sclerosis complex), in the size of its subunits, the location of the GAP domain, and its phosphorylation by Akt.]. 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:16490346
;
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:NP161350.RA2ehzYN8cor9FWwp9NhHpXA8ukPXHxvYMry7WOeeQmoI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}