@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE
> .
@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:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_head
{
this:
np:hasAssertion
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_assertion
;
np:hasProvenance
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_provenance
;
np:hasPublicationInfo
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_assertion
a
np:Assertion
.
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_provenance
a
np:Provenance
.
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_assertion
{
miriam-gene:2146
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNb807eca378dd0bb29898dbaa8a5a15e3
sio:SIO_000628
miriam-gene:2146
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_provenance
{
dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_assertion
dcterms:description
"[Recent extensive mutation analyses of the myeloid malignancies have revealed that inactivating somatic mutations in PcG genes such as EZH2 and ASXL1 occur frequently in patients with myelodysplastic disorders including myelodysplastic syndromes (MDSs) and MDS/myeloproliferative neoplasm (MPN) overlap disorders (MDS/MPN).]. 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:24218139
;
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:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}