@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A130_assertion
;
np:hasProvenance
dgn-np:NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A130_provenance
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np:hasPublicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A130_provenance
a
np:Provenance
.
dgn-np:NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A130_publicationInfo
a
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.
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dgn-np:NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0024282
a
ncit:C7057
.
dgn-gda:DGN3c0122409cbe85c0a5d74d65c1caf77d
sio:SIO_000628
miriam-gene:595
,
lld:C0024282
;
a
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.
}
dgn-np:NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A130_provenance
{
dgn-np:NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A130_assertion
dcterms:description
"[We arrived at the following conclusions: (a) FISH with this BCL1 YAC probe is an efficient method for the detection of the t(11;14) and of the corresponding involvement of the BCL1 locus in this lymphoproliferative disorder; (b) the majority of BCL1-positive atypical CLLs by French-American-British criteria may carry 13q14 deletions; (c) the recognition of this cytogenetic subset of atypical CLL, sharing some immunological and cytogenetic features with mantle cell lymphoma, may be important, because these patients usually present isolated peripheral blood and marrow lymphocytosis, with or without mild to moderate spleen involvement, and may require early cytotoxic treatment.]. 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:9067285
;
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:NP762561.RAF5bsEcg-UFNoX4g_cvEi9u4ouj4MZEY3ivOTbKLBd2A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+02:00"^^
xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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}