@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys
> .
@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/v3.0.0/void/
> .
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_head
{
this:
np:hasAssertion
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_assertion
;
np:hasProvenance
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_provenance
;
np:hasPublicationInfo
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_assertion
a
np:Assertion
.
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_provenance
a
np:Provenance
.
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0699790
a
ncit:C7057
.
dgn-gda:DGN409f1113e6d92c820da960b47859d38e
sio:SIO_000628
miriam-gene:5624
,
lld:C0699790
;
a
sio:SIO_001121
.
}
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_provenance
{
dgn-np:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP648521.RAHo2bw4yGcoC3x0qSLfY_ZXRX8CigztpNfwq21v_16Ys130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:09+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}