@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4
> .
@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:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_head
{
this:
np:hasAssertion
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_assertion
;
np:hasProvenance
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_provenance
;
np:hasPublicationInfo
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_assertion
a
np:Assertion
.
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_provenance
a
np:Provenance
.
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN696f1f78269f79dad42174554c3a7ccc
sio:SIO_000628
miriam-gene:324
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_provenance
{
dgn-np:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_assertion
dcterms:description
"[The low frequency of CTNNB1 mutations, however, suggests that mutation of another Wnt signaling component, such as the Wnt scaffolding protein axin or the adenomatous polyposis coli protein, both of which modulate beta-catenin stability, also may be involved in aflatoxin-associated HCC.]. 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:11429783
;
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:NP658887.RAfg_d2ypHNlCwQlPULq7jVCaHfPbDTzlhgEAgOy40ci4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:38+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" .
}