@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA
> .
@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:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_head
{
this:
np:hasAssertion
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_assertion
;
np:hasProvenance
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_provenance
;
np:hasPublicationInfo
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_assertion
a
np:Assertion
.
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_provenance
a
np:Provenance
.
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_assertion
{
miriam-gene:6343
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGNff237e0ab4edc45761e2c460c23b4da7
sio:SIO_000628
miriam-gene:6343
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_provenance
{
dgn-np:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_assertion
dcterms:description
"[Allogeneic hematopoietic stem cell transplantation (SCT) is well accepted as a curative treatment approach for younger patients with myelodysplastic syndrome (MDS) and has become one of the most frequent indications for allogeneic SCT as reported to the Center for International Blood and Marrow Transplant Research.]. 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:22504927
;
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:NP931447.RA82D1kNAlNSLVJJD8DPuKu5kTgjS0QxtDxh-zzIMZ2GA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}