@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_assertion
a
np:Assertion
.
dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_provenance
a
np:Provenance
.
dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN5ac688c45c4e4712469cc90d378d9c23
sio:SIO_000628
miriam-gene:1029
,
lld:C0026986
;
a
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.
}
dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_provenance
{
dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_assertion
dcterms:description
"[We studied the methylation status of the p15(INK4B) and p16(INK4A) genes in 47 pediatric patients with primary MDS, its correlation with subtype, and the role of p15(INK4B) and p16(INK4A) in the evolution of MDS toward AML.]. 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:20658957
;
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 .
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dgn-np:NP668503.RAbc2LTuf15P3dWRt6vRyWsOjsyCuMaDQcXq75i96OOz4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:43+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
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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