@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU
> .
@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:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_head
{
this:
np:hasAssertion
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_assertion
;
np:hasProvenance
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_provenance
;
np:hasPublicationInfo
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_assertion
a
np:Assertion
.
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_provenance
a
np:Provenance
.
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_assertion
{
miriam-gene:604
a
ncit:C16612
.
lld:C0280803
a
ncit:C7057
.
dgn-gda:DGN463182d9627a444c07894fd9edfd6293
sio:SIO_000628
miriam-gene:604
,
lld:C0280803
;
a
sio:SIO_001121
.
}
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_provenance
{
dgn-np:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_assertion
dcterms:description
"[Chromosomal translocations fusing the BCL6 gene to different partner loci are recurrent in primary central nervous system lymphoma and may be associated with aberrant somatic hypermutation or defective class switch recombination.]. 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:16896311
;
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:NP195478.RA_De-eZxDzg_d9kiC0VTf-s1TuOWujyYdovlowZ2-NgU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}