@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY
> .
@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:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_head
{
this:
np:hasAssertion
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_assertion
;
np:hasProvenance
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_provenance
;
np:hasPublicationInfo
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_assertion
a
np:Assertion
.
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_provenance
a
np:Provenance
.
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0242596
a
ncit:C7057
.
dgn-gda:DGN5fc1cfc947899fd491aa9701ffa80302
sio:SIO_000628
miriam-gene:1029
,
lld:C0242596
;
a
sio:SIO_001121
.
}
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_provenance
{
dgn-np:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_assertion
dcterms:description
"[To investigate the frequency of p15 and p16 gene promoter methylation in acute promyelocytic leukemia (APL), and to define its value in the detection of minimal residual disease (MRD) and treatment prognostication.]. 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:11283136
;
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:NP500039.RADfywjIR2OWBHNYpxjzjFi1y9xuwdOo_2nfGvIRpyeOY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}