@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ
> .
@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:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_head
{
this:
np:hasAssertion
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_assertion
;
np:hasProvenance
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_assertion
a
np:Assertion
.
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_provenance
a
np:Provenance
.
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C0002894
a
ncit:C7057
.
dgn-gda:DGNbcb6eb6f49f710275163c9608cc73b6b
sio:SIO_000628
miriam-gene:861
,
lld:C0002894
;
a
sio:SIO_001121
.
}
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_provenance
{
dgn-np:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_assertion
dcterms:description
"[AML1/RUNX1 mutations have been reported frequently in myelodysplastic syndrome (MDS) patients, especially those diagnosed with refractory anemia with excess blast (RAEB), RAEB in transformation (RAEBt), or AML following MDS (these categories are defined as MDS/AML).]. 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:16467864
;
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:NP225020.RA-RnPCHX2QieH2IKLs8b3RIsWW0D6CdREgZb_flU5llQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}