@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ
> .
@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:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_head
{
this:
np:hasAssertion
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_assertion
;
np:hasProvenance
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_assertion
a
np:Assertion
.
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_provenance
a
np:Provenance
.
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_assertion
{
miriam-gene:7704
a
ncit:C16612
.
lld:C2745900
a
ncit:C7057
.
dgn-gda:DGNc27b4fb4b92f13d5533ca1493b1dea58
sio:SIO_000628
miriam-gene:7704
,
lld:C2745900
;
a
sio:SIO_001121
.
}
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_provenance
{
dgn-np:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_assertion
dcterms:description
"[Some APL cases also involve rearrangements that fuse RAR to partner genes other than PML, including nucleophosmin (NPM), promyelocytic leukemia zinc finger (PLZF), nuclear mitotic apparatus (NUMA), and Stat5b, but the clinical characteristics of APL without PML-RAR have not been fully clarified.]. 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:17988991
;
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:NP324818.RAWtGpMype3ATR1JNIi5trX8TuRL9D5vpAqrTaz5-hIlQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}