@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ
> .
@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:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_head
{
this:
np:hasAssertion
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_assertion
;
np:hasProvenance
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_assertion
a
np:Assertion
.
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_provenance
a
np:Provenance
.
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C0023480
a
ncit:C7057
.
dgn-gda:DGNa7936a5d4f099d345cde53939c7cb488
sio:SIO_000628
miriam-gene:2187
,
lld:C0023480
;
a
sio:SIO_001121
.
}
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_provenance
{
dgn-np:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_assertion
dcterms:description
"[Five patients had myelodysplastic syndrome (MDS) diagnosed according to the FAB nomenclature as chronic myelomonocytic leukemia (CMML) in two cases, refractory anemia with excess of blasts in transformation (RAEBt) in two cases, and refractory anemia with excess of blasts (RAEB) in one case.]. 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:2328318
;
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:NP436587.RACtfXNiW5nRHoY1oQRqdxYeIktNKc4GT_BiSjBPvmkFQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}