@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg
> .
@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:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_head
{
this:
np:hasAssertion
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_assertion
;
np:hasProvenance
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_provenance
;
np:hasPublicationInfo
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_assertion
a
np:Assertion
.
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_provenance
a
np:Provenance
.
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_assertion
{
miriam-gene:5371
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNf746943018af0023d9efbeed91729825
sio:SIO_000628
miriam-gene:5371
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_provenance
{
dgn-np:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_assertion
dcterms:description
"[Our results suggest that interference with retinoid signalling, and not disruption of PML organization, is essential to the APL phenotype and implicates for the first time an element of the mitotic apparatus in the molecular pathogenesis of human malignancy.]. 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:9288109
;
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:NP251321.RAJB9XETFsN33Fr4t4KtbtvTCwgdHnZmIcx-q7q4RuULg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}