@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg
> .
@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:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_head
{
this:
np:hasAssertion
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_assertion
;
np:hasProvenance
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_provenance
;
np:hasPublicationInfo
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_assertion
a
np:Assertion
.
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_provenance
a
np:Provenance
.
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0474808
a
ncit:C7057
.
dgn-gda:DGN0158e8321c7a9f6df8f1a7bb72322bb1
sio:SIO_000628
miriam-gene:1029
,
lld:C0474808
;
a
sio:SIO_001121
.
}
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_provenance
{
dgn-np:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_assertion
dcterms:description
"[Sequential samples of the indolent and transformed phase of three cases showed the presence of p16(INK4a) deletions in the Richter's syndrome but not in the CLL component of two cases, whereas in a follicular lymphoma the deletion was present in both the follicular tumor and in the diffuse large-cell lymphoma.]. 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:9531609
;
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:NP882474.RAaaZEW7Hsn1BI7JHR71vDTsaIAdR5DRo6ixVDefm6xBg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}