@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4
> .
@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:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_head
{
this:
np:hasAssertion
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_assertion
;
np:hasProvenance
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_provenance
;
np:hasPublicationInfo
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_assertion
a
np:Assertion
.
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_provenance
a
np:Provenance
.
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_assertion
{
miriam-gene:2146
a
ncit:C16612
.
lld:C0023470
a
ncit:C7057
.
dgn-gda:DGN51fe78cb20ba60e9e75740711696c2f6
sio:SIO_000628
miriam-gene:2146
,
lld:C0023470
;
a
sio:SIO_001121
.
}
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_provenance
{
dgn-np:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_assertion
dcterms:description
"[Finally, the nature of the EZH2 protein and its mapping to the critical region for malignant myeloid disorders lead us to propose the EZH2 gene is involved in the pathogenesis of 7q35-q36 aberrations in myeloid leukaemia.]. 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:10780782
;
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:NP414486.RAlYLzfC7IONPE9Fky-MA0kB8D79YamWLxTqC9mCMcth4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:06+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" .
}