@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk
> .
@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:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_head
{
this:
np:hasAssertion
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_assertion
;
np:hasProvenance
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_provenance
;
np:hasPublicationInfo
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_assertion
a
np:Assertion
.
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_provenance
a
np:Provenance
.
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_assertion
{
miriam-gene:4851
a
ncit:C16612
.
lld:C1516669
a
ncit:C7057
.
dgn-gda:DGN0cd0bf400fe91ea7fb2b18f7e94e829d
sio:SIO_000628
miriam-gene:4851
,
lld:C1516669
;
a
sio:SIO_001121
.
}
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_provenance
{
dgn-np:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_assertion
dcterms:description
"[The aim of this study was to determine the incidence, and biological significance of clonal evolution (CE) using conventional and molecular cytogenetics and its relationship with prognostic markers such as CD38, ZAP70, and the mutational status of IGHV and NOTCH1.]. 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:23893575
;
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:NP168969.RAw3KZb0R1ahC_rE5YPMkptjpNhtMB3tOWayYlFDMyhkk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}