@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y
> .
@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:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_head
{
this:
np:hasAssertion
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_assertion
;
np:hasProvenance
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_assertion
a
np:Assertion
.
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_provenance
a
np:Provenance
.
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN1eb8b78377b98dc6d87194aa534185cd
sio:SIO_000628
miriam-gene:3342
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_provenance
{
dgn-np:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_assertion
dcterms:description
"[The aim of this study was to apply comparative genomic hybridization (CGH) to cases of AML or MDS in transformation submitted for routine cytogenetic analysis to investigate whether this approach would yield any further information and, if possible, to predict which cases would benefit from CGH analysis.]. 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:11343775
;
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:NP684339.RAqDqUpSM0aqOp_IkVEZcJ0e4SYkTXXtUnQqtlTb-fC3Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}