@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1095571.RAPLRPVqXgnJmX7t1NaEKTs4bzWBvVemvuUSMOEjSWpHI
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP1095571.RAPLRPVqXgnJmX7t1NaEKTs4bzWBvVemvuUSMOEjSWpHI130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1095571.RAPLRPVqXgnJmX7t1NaEKTs4bzWBvVemvuUSMOEjSWpHI130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP1095571.RAPLRPVqXgnJmX7t1NaEKTs4bzWBvVemvuUSMOEjSWpHI130_assertion
a
np:Assertion
.
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a
np:Provenance
.
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.
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{
miriam-gene:3492
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNfa89af61c7acfe0d9aec634453587a70
sio:SIO_000628
miriam-gene:3492
,
lld:C0023418
;
a
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.
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dgn-np:NP1095571.RAPLRPVqXgnJmX7t1NaEKTs4bzWBvVemvuUSMOEjSWpHI130_provenance
{
dgn-np:NP1095571.RAPLRPVqXgnJmX7t1NaEKTs4bzWBvVemvuUSMOEjSWpHI130_assertion
dcterms:description
"[We identified a novel t(10;14)(p12;q32)/IGH-BMI1 rearrangement and its IGL variant in six cases of chronic lymphocytic leukemia (CLL) and found that these aberrations were consistently acquired at time of disease progression and high grade transformation of leukemia (Richter syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:23873701
;
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 .
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dgn-np:NP1095571.RAPLRPVqXgnJmX7t1NaEKTs4bzWBvVemvuUSMOEjSWpHI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:02+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v4.0.0" .
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