@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU
> .
@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:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_head
{
this:
np:hasAssertion
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_assertion
;
np:hasProvenance
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_provenance
;
np:hasPublicationInfo
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_assertion
a
np:Assertion
.
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_provenance
a
np:Provenance
.
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0376544
a
ncit:C7057
.
dgn-gda:DGN5a649298a6fa7a7cbf62c270de2d3e71
sio:SIO_000628
miriam-gene:1029
,
lld:C0376544
;
a
sio:SIO_001121
.
}
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_provenance
{
dgn-np:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_assertion
dcterms:description
"[The purpose of this study is to figure out the precise manners and frequencies of p16 gene inactivation in diverse hematopoietic tumor types and thus to clarify its significance in development of human hematopoietic malignancies.]. 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:7632963
;
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:NP866033.RA_SOl2QRSVPVG02F0qLy8d9ttNDupq8QnaYealL5JYjU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:49+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" .
}