@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI
> .
@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:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_head
{
this:
np:hasAssertion
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_assertion
;
np:hasProvenance
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_provenance
;
np:hasPublicationInfo
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_assertion
a
np:Assertion
.
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_provenance
a
np:Provenance
.
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_assertion
{
miriam-gene:10058
a
ncit:C16612
.
lld:C1333295
a
ncit:C7057
.
dgn-gda:DGN8df28ef80f0604a93df13512d5d98a22
sio:SIO_000628
miriam-gene:10058
,
lld:C1333295
;
a
sio:SIO_001121
.
}
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_provenance
{
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_assertion
dcterms:description
"[A comparison of genome profiles of distinct subgroups of DLBCL demonstrated that (1) ABC DLBCL is characterized by gain of 3q, 18q, and 19q and loss of 6q and 9p21, and GCB DLBCL is characterized by gain of 1q, 2p, 7q, and 12q; (2) the genomic imbalances characteristic of the CD5(+) and CD5(-)CD10(+) groups were similar to those of the ABC and GCB types, respectively.]. 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:15886317
;
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:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}