@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4
> .
@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:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_head
{
this:
np:hasAssertion
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_assertion
;
np:hasProvenance
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_provenance
;
np:hasPublicationInfo
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_assertion
a
np:Assertion
.
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_provenance
a
np:Provenance
.
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0349631
a
ncit:C7057
.
dgn-gda:DGNa39077c3995b67d59439b2caef089e0f
sio:SIO_000628
miriam-gene:1029
,
lld:C0349631
;
a
sio:SIO_001121
.
}
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_provenance
{
dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_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:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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" .
}