@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4
> .
@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:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_head
{
this:
np:hasAssertion
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_assertion
;
np:hasProvenance
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_provenance
;
np:hasPublicationInfo
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_assertion
a
np:Assertion
.
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_provenance
a
np:Provenance
.
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1516669
a
ncit:C7057
.
dgn-gda:DGN69dc43d4138b09fc9cce6e6b4692a12f
sio:SIO_000628
miriam-gene:7157
,
lld:C1516669
;
a
sio:SIO_001121
.
}
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_provenance
{
dgn-np:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_assertion
dcterms:description
"[To better define the significance of clonal evolution (CE) including 14q32 translocations involving the immunoglobulin heavy chain gene (IGH) in chronic lymphocytic leukemia (CLL), 105 patients were analyzed sequentially by fluorescence in situ hybridization (FISH) with the following panel of probes: 13q14/D13S25, 11q22/ATM, 17p13/TP53, #12-centromere and 14q32/IGH break-apart probe.]. 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:21767243
;
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:NP467288.RAQak2HlzAk5WLiI-D1jy1qxDqm_VWrZbcu6CapykB1X4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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" .
}