@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os
> .
@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/v4.0.0/void/
> .
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_head
{
this:
np:hasAssertion
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_assertion
;
np:hasProvenance
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_provenance
;
np:hasPublicationInfo
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_assertion
a
np:Assertion
.
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_provenance
a
np:Provenance
.
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_assertion
{
miriam-gene:5715
a
ncit:C16612
.
lld:C0023493
a
ncit:C7057
.
dgn-gda:DGNed294ff5477cb2b2e25fb048cea006cc
sio:SIO_000628
miriam-gene:5715
,
lld:C0023493
;
a
sio:SIO_001121
.
}
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_provenance
{
dgn-np:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_assertion
dcterms:description
"[Although genetic alterations of p18, p19, p21, p27 have rarely been reported, inactivation of these genes may contribute to the development of ATLL because low expression levels of these genes seem to mark ATLL.]. 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:12040438
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP356597.RA4VBZQqgUK09OcBRezNLYiEyGvrglMQRrZwaIgO2l5os130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:27+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}