@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_head
{
this:
np:hasAssertion
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_assertion
;
np:hasProvenance
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_provenance
;
np:hasPublicationInfo
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_assertion
a
np:Assertion
.
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_provenance
a
np:Provenance
.
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_assertion
{
miriam-gene:3492
a
ncit:C16612
.
lld:C1840451
a
ncit:C7057
.
dgn-gda:DGNb652904cc435a22af15a653d3209585a
sio:SIO_000628
miriam-gene:3492
,
lld:C1840451
;
a
sio:SIO_001121
.
}
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_provenance
{
dgn-np:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP486582.RAS5MSGtExNU7EGBxjyB9f_lwLXljjO8rFhUSqVqlPrio130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:27+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}