@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck
> .
@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:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_head
{
this:
np:hasAssertion
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_assertion
;
np:hasProvenance
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_provenance
;
np:hasPublicationInfo
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_assertion
a
np:Assertion
.
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_provenance
a
np:Provenance
.
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0699790
a
ncit:C7057
.
dgn-gda:DGN252c6842c33cd02c26ef2e6efe4af66a
sio:SIO_000628
miriam-gene:324
,
lld:C0699790
;
a
sio:SIO_001121
.
}
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_provenance
{
dgn-np:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_assertion
dcterms:description
"[Mutations in APC or CTNNB1 are highly frequent in colon cancer and cause aberrant stabilization of CTNNB1, which activates the transcription of Wnt target genes by binding to chromatin via the TCF/LEF transcription factors.]. 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:24651522
;
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:NP1165861.RAnBUZXx2SW-SG6Mcrtjb6P7N4Hek4TR3juRDXbwW0Fck130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:34+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" .
}