@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI
> .
@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:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_head
{
this:
np:hasAssertion
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_assertion
;
np:hasProvenance
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_provenance
;
np:hasPublicationInfo
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_assertion
a
np:Assertion
.
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_provenance
a
np:Provenance
.
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_assertion
{
miriam-gene:4353
a
ncit:C16612
.
lld:C0398595
a
ncit:C7057
.
dgn-gda:DGNc9bd78e23751d49f477c3d8b594a94e5
sio:SIO_000628
miriam-gene:4353
,
lld:C0398595
;
a
sio:SIO_001121
.
}
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_provenance
{
dgn-np:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_assertion
dcterms:description
"[Myelodysplastic features and myeloperoxidase (MPO) deficiency have been investigated in a series of 336 cases of de novo acute myeloid leukemia (AML) to clarify their impact on the outcome of such patients and to compare with the previous results from the literature.]. 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:1318461
;
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:NP781387.RAPzKqW4KV946fsZ6B_DE-1wV9IYh2_hE3stDEFL2_7tI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}