@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP426426.RA7P1ywSTcTk0oEn1cTvJv6hJI48FYI0WPn6X51muWc0w
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP426426.RA7P1ywSTcTk0oEn1cTvJv6hJI48FYI0WPn6X51muWc0w130_assertion
;
np:hasProvenance
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;
a
np:Nanopublication
.
dgn-np:NP426426.RA7P1ywSTcTk0oEn1cTvJv6hJI48FYI0WPn6X51muWc0w130_assertion
a
np:Assertion
.
dgn-np:NP426426.RA7P1ywSTcTk0oEn1cTvJv6hJI48FYI0WPn6X51muWc0w130_provenance
a
np:Provenance
.
dgn-np:NP426426.RA7P1ywSTcTk0oEn1cTvJv6hJI48FYI0WPn6X51muWc0w130_publicationInfo
a
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.
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{
miriam-gene:51639
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN48a43f1356fed5fd92141f0ea2cfcdc2
sio:SIO_000628
miriam-gene:51639
,
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;
a
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.
}
dgn-np:NP426426.RA7P1ywSTcTk0oEn1cTvJv6hJI48FYI0WPn6X51muWc0w130_provenance
{
dgn-np:NP426426.RA7P1ywSTcTk0oEn1cTvJv6hJI48FYI0WPn6X51muWc0w130_assertion
dcterms:description
"[We performed a comprehensive analysis of the deletion and the methylation profile of CDKN2A (hereafter identified separately as p16 and p14, for the different proteins encoded) and CDKN2B (hereafter p15) in 91 newly diagnosed B-ALL patients (61 children, 30 adults).]. 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:19837270
;
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:NP426426.RA7P1ywSTcTk0oEn1cTvJv6hJI48FYI0WPn6X51muWc0w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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dgn-void:disgenetrdf
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}