@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w
> .
@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:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_head
{
this:
np:hasAssertion
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_assertion
;
np:hasProvenance
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_provenance
;
np:hasPublicationInfo
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_assertion
a
np:Assertion
.
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_provenance
a
np:Provenance
.
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_assertion
{
miriam-gene:6343
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNf107b9037128e0a18445755a69a6525f
sio:SIO_000628
miriam-gene:6343
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_provenance
{
dgn-np:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_assertion
dcterms:description
"[Allogeneic hematopoietic SCT (allo-HCT) from matched sibling donor (MSD) is recommended for younger patients with intermediate cytogenetic risk AML in first CR (CR1), whereas the role of alternative donor transplants in these patients is unknown.]. 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:22705800
;
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:NP429642.RA4nZufniQG9GjuDbfWAlaiWNEAWREHiOoo-pEmT0se2w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}