@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg
> .
@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:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_head
{
this:
np:hasAssertion
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_assertion
;
np:hasProvenance
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_provenance
;
np:hasPublicationInfo
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_assertion
a
np:Assertion
.
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_provenance
a
np:Provenance
.
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_assertion
{
miriam-gene:29107
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN131aa4ae14df3f8a6f0e76fc26d36d0f
sio:SIO_000628
miriam-gene:29107
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_provenance
{
dgn-np:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_assertion
dcterms:description
"[Several genes and gene pathways disrupted by aberrant CpG island methylation have now been identified in haematological malignancies, the most frequently studied being the cell cycle inhibitors p16 (now termed CDKN2A; mostly methylated in lymphoid malignancy) and p15 (now termed CDKN2B; commonly methylated in lymphoid and myeloid 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:17489980
;
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:NP696691.RA09QIEqlEGMtrndKVh4EaX66-W0wteU-m_xFhq99WIhg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}