@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE
> .
@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:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_head
{
this:
np:hasAssertion
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_assertion
;
np:hasProvenance
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_provenance
;
np:hasPublicationInfo
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_assertion
a
np:Assertion
.
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_provenance
a
np:Provenance
.
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_assertion
{
miriam-gene:10153
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNe2b9c3e35e66a40497952d034ac56817
sio:SIO_000628
miriam-gene:10153
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_provenance
{
dgn-np:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_assertion
dcterms:description
"[Among AML cases with a favourable karyotype, hypermethylation of SFRP genes was restricted to patients with core binding factor (CBF) leukaemia, and aberrant methylation of the SFRP2 promoter was an adverse risk factor for survival in CBF leukaemia.]. 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:18537968
;
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:NP175784.RAqeWe4oDxJ69-YI0iGpqjuhi-s8ZwpTUd40ydk26AQYE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}