@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4
> .
@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:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_head
{
this:
np:hasAssertion
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_assertion
;
np:hasProvenance
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_provenance
;
np:hasPublicationInfo
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_assertion
a
np:Assertion
.
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_provenance
a
np:Provenance
.
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_assertion
{
miriam-gene:5914
a
ncit:C16612
.
lld:C0023487
a
ncit:C7057
.
dgn-gda:DGNa2622a92bad4aac97edf711a85827597
sio:SIO_000628
miriam-gene:5914
,
lld:C0023487
;
a
sio:SIO_001121
.
}
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_provenance
{
dgn-np:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_assertion
dcterms:description
"[Apart from a well-known FC pattern of hypergranular APL, we presented less common immunophenotypic variants of APL, which helps to identify an additional group of patients who would benefit from fast confirmatory FISH and/or PCR testing for t(15;17)/PML-RARA.]. 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:22535601
;
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:NP176552.RA2IwRtsuP6A2NGve9YT_ot-H7siZp0zH7SSsE9E-T0Z4130_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" .
}