@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM
> .
@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:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_head
{
this:
np:hasAssertion
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_assertion
;
np:hasProvenance
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_provenance
;
np:hasPublicationInfo
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_assertion
a
np:Assertion
.
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_provenance
a
np:Provenance
.
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNf732cafd78940cb004dc7c21c5ad599f
sio:SIO_000628
miriam-gene:1499
,
lld:C0596263
;
a
sio:SIO_001122
.
}
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_provenance
{
dgn-np:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_assertion
dcterms:description
"[A recent study has shown that about half of the sporadic CRC lacking APC mutation has CTNNB1 mutation, suggesting that CTNNB1 mutation can substitute for APC mutation in the initiation of colorectal tumorigenesis.]. 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:10398435
;
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:NP257139.RARmXth3eDH87uVzEcIEkfTW6P1E910ineyMJ7ijOI2JM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:42+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" .
}