@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30
> .
@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:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_head
{
this:
np:hasAssertion
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_assertion
;
np:hasProvenance
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_provenance
;
np:hasPublicationInfo
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_assertion
a
np:Assertion
.
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_provenance
a
np:Provenance
.
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_assertion
{
miriam-gene:3492
a
ncit:C16612
.
lld:C0242596
a
ncit:C7057
.
dgn-gda:DGN69ea43c2dcf6d6af95fccfb205dd3298
sio:SIO_000628
miriam-gene:3492
,
lld:C0242596
;
a
sio:SIO_001121
.
}
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_provenance
{
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_assertion
dcterms:description
"[This is because the issue of the benefits of achieving MRD-negative status in patients with CLL requires further investigation in large controlled trials, in which patients should be stratified according to not only clinical variables but also biological parameters such as cytogenetics, IGHV mutations or ZAP-70 expression.]. 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:20620974
;
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:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}