@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg
> .
@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:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_head
{
this:
np:hasAssertion
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_assertion
;
np:hasProvenance
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_provenance
;
np:hasPublicationInfo
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_assertion
a
np:Assertion
.
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_provenance
a
np:Provenance
.
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_assertion
{
miriam-gene:6423
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN583584d900864949ffe4cebf01f77237
sio:SIO_000628
miriam-gene:6423
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_provenance
{
dgn-np:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_assertion
dcterms:description
"[In patients with AML with normal cytogenetics, sFRP2 and sFRP5 methylation at the time of diagnosis was associated with an increased risk of relapse, and sFRP2 methylation was associated with an increased risk for death.]. 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:20795789
;
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:NP479647.RA3nS0IOeY8Ztq19thhYd4L5HWGSLM7og4QgDNfdSwaEg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}