@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg
> .
@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:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_head
{
this:
np:hasAssertion
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_assertion
;
np:hasProvenance
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_provenance
;
np:hasPublicationInfo
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_assertion
a
np:Assertion
.
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_provenance
a
np:Provenance
.
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C2981142
a
ncit:C7057
.
dgn-gda:DGN524d5f697fa9c00068d82e9cba153618
sio:SIO_000628
miriam-gene:2187
,
lld:C2981142
;
a
sio:SIO_001121
.
}
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_provenance
{
dgn-np:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_assertion
dcterms:description
"[Improvement of criteria for refractory cytopenia with multilineage dysplasia according to the WHO classification based on prognostic significance of morphological features in patients with refractory anemia according to the FAB classification.]. 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:17268513
;
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:NP809557.RA3BtZ481aAyHALx6Wj4Obdw7kyKBL8TMuVSzJF7iapKg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}