@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y
> .
@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:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_head
{
this:
np:hasAssertion
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_assertion
;
np:hasProvenance
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_assertion
a
np:Assertion
.
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_provenance
a
np:Provenance
.
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_assertion
{
miriam-gene:1044
a
ncit:C16612
.
lld:C0004763
a
ncit:C7057
.
dgn-gda:DGN80caf2c48da8a771fb6b61b52a4b51ee
sio:SIO_000628
miriam-gene:1044
,
lld:C0004763
;
a
sio:SIO_001121
.
}
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_provenance
{
dgn-np:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_assertion
dcterms:description
"[Although the initial trigger for CDX1 promoter demethylation is not yet identified, it seems likely that demethylation of its promoter may be the key to the induction and maintenance of CDX1 expression and so of the BM phenotype.]. 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:15894614
;
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:NP704944.RAew7bqXkxZFZ49hha91IEEOEs6Typ53Rpi_NSETDvJ8Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:08+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" .
}