@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g
> .
@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:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_head
{
this:
np:hasAssertion
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_assertion
;
np:hasProvenance
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_provenance
;
np:hasPublicationInfo
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_assertion
a
np:Assertion
.
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_provenance
a
np:Provenance
.
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_assertion
{
miriam-gene:2146
a
ncit:C16612
.
lld:C0027962
a
ncit:C7057
.
dgn-gda:DGN3c44e5edf497995ff81d57a9ae153f3a
sio:SIO_000628
miriam-gene:2146
,
lld:C0027962
;
a
sio:SIO_001121
.
}
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_provenance
{
dgn-np:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_assertion
dcterms:description
"[In this study, we report that EZH2, which we find absent in melanocytic nevi but expressed in many or most metastatic melanoma cells, functionally suppresses the senescent state in human melanoma cells.]. 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:21383005
;
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:NP729079.RA9_ryUBOr7Om0wNs_zNc8Qj6klcvQMYn357N87DDqi-g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+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" .
}