@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0
> .
@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:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_head
{
this:
np:hasAssertion
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_assertion
;
np:hasProvenance
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_provenance
;
np:hasPublicationInfo
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_assertion
a
np:Assertion
.
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_provenance
a
np:Provenance
.
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_assertion
{
miriam-gene:1786
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN2c5fc0a90a316f2ef7550a79a8b3106b
sio:SIO_000628
miriam-gene:1786
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_provenance
{
dgn-np:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_assertion
dcterms:description
"[The present study was designed to investigate the potential relationship between CDKN2A (p16) gene hypermethylation, which has reported to be frequently observed in oral squamous cell carcinomas (OSCCs), and expression of human DNA methyltransferases (DNMTs: DNMT1, DNMT3A and DNMT3B).]. 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:12738984
;
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:NP508325.RADU6CDyTeWraPKqI32MyU2IKn7Hj05xegHd03PU-aqn0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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
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dgn-void:disgenetrdf
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}