@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI
> .
@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:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_head
{
this:
np:hasAssertion
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_assertion
;
np:hasProvenance
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_provenance
;
np:hasPublicationInfo
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_assertion
a
np:Assertion
.
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_provenance
a
np:Provenance
.
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_assertion
{
miriam-gene:84106
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN88ae189d9039b4b117e842dc3386f52a
sio:SIO_000628
miriam-gene:84106
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_provenance
{
dgn-np:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_assertion
dcterms:description
"[These results indicate that qrtPCR monitoring of PML-RAR alpha NQ can identify patients at high risk of relapse and suggest that clinically practical PB NQ monitoring at more frequent FUP intervals may improve predictive accuracy for relapse or continuing CR in patients with persistent, fluctuating minimal residual disease levels.]. 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:12468436
;
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:NP353595.RA3IcdY-TGeQv9MEjSgst-LbZ0zvgm41iZg3yJlTs8BAI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}