@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8
> .
@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/v3.0.0/void/
> .
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_head
{
this:
np:hasAssertion
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_assertion
;
np:hasProvenance
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_provenance
;
np:hasPublicationInfo
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_assertion
a
np:Assertion
.
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_provenance
a
np:Provenance
.
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGNc409232b102afdeb0e10ada22df14389
sio:SIO_000628
miriam-gene:5925
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_provenance
{
dgn-np:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_assertion
dcterms:description
"[Our data suggest that the clinical course of CLL is accelerated in patients with large (type II) 13q14 deletions that span the RB1 gene, therefore justifying routine identification of 13q14 subtypes in CLL management.]. 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:21890456
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP666874.RA2Cpv9dkoj-2ENtU-Tjl9tJfYPm9Bz71vcj96fCPcjn8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:20+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}