@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc
> .
@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:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_head
{
this:
np:hasAssertion
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_assertion
;
np:hasProvenance
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_provenance
;
np:hasPublicationInfo
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_assertion
a
np:Assertion
.
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_provenance
a
np:Provenance
.
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGNa8aad590ed5f23f156596ba8f160b103
sio:SIO_000628
miriam-gene:1030
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_provenance
{
dgn-np:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_assertion
dcterms:description
"[These findings indicate that deletion of the p16INK4a/p15INK4b locus is one of the most common genetic abnormalities so far detected in pediatric ALL, and that loss of one or more of these cell cycle kinase inhibitors is important in leukemogenesis.]. 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:7727766
;
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:NP264524.RAKdbG9ZzgmZagi6OhZceuy2dXULXEMXMiXNW_LxwSkYc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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: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" .
}