@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4
> .
@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:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_head
{
this:
np:hasAssertion
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_assertion
;
np:hasProvenance
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_provenance
;
np:hasPublicationInfo
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_assertion
a
np:Assertion
.
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_provenance
a
np:Provenance
.
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_assertion
{
miriam-gene:2146
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN84d9f115f356bb4cff5600fe4b991f42
sio:SIO_000628
miriam-gene:2146
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_provenance
{
dgn-np:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_assertion
dcterms:description
"[Aberrant differentiation in MDS can often be traced to abnormal DNA methylation (both gains and losses of DNA methylation genome wide and at specific loci) as well as mutations in genes that regulate epigenetic programs (TET2 and DNMT3a, both involved in DNA methylation control; EZH2 and ASXL1, both involved in histone methylation control).]. 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:23660859
;
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:NP291723.RAhXKrqzOJ80XvdyUjzYfIkEuLokNz0WL086IBGqrGix4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}