@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4
> .
@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:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_head
{
this:
np:hasAssertion
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_assertion
;
np:hasProvenance
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_provenance
;
np:hasPublicationInfo
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_assertion
a
np:Assertion
.
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_provenance
a
np:Provenance
.
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_assertion
{
miriam-gene:6935
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNa9ace4257191cd60bbe5fcf873d9f7b2
sio:SIO_000628
miriam-gene:6935
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_provenance
{
dgn-np:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_assertion
dcterms:description
"[In conclusion, in colorectal cancer, the 73 bp deletion in the first intron of the p73 gene and different expression levels of ZEB1 and p300 may act in concert to affect the ratio of TAp73/DeltaTAp73 forms, favouring p73 oncogenic variants.]. 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:17029218
;
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:NP156678.RAh44MLUCZeay3Z7rIql-e3X__hPx9JPUivGKUQn3Blk4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}