@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_head
{
this:
np:hasAssertion
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_assertion
;
np:hasProvenance
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_provenance
;
np:hasPublicationInfo
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_assertion
a
np:Assertion
.
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_provenance
a
np:Provenance
.
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_assertion
{
miriam-gene:5914
a
ncit:C16612
.
lld:C0023487
a
ncit:C7057
.
dgn-gda:DGN16c3b31bc5ffb1f169c41016136cb605
sio:SIO_000628
miriam-gene:5914
,
lld:C0023487
;
a
sio:SIO_001121
.
}
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_provenance
{
dgn-np:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_assertion
dcterms:description
"[These data, along with previous reports of rare variant translocations in APL, indicate that while dysregulation of RARA by gene fusion may be essential for the APL phenotype, the particular fusion partner may determine clinicopathological aspects, including presentation, response to treatment with all-trans retinoic acid (ATRA), and prognosis.]. 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:8618456
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1348637.RArBb7CfZRTVkcXVpIDK3FoyBWtLFtko7_7kL_C6vRv7E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:57+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}