@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4
> .
@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:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_head
{
this:
np:hasAssertion
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_assertion
;
np:hasProvenance
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_provenance
;
np:hasPublicationInfo
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_assertion
a
np:Assertion
.
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_provenance
a
np:Provenance
.
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN38541aebdb9362f15b1fb0e173950b55
sio:SIO_000628
miriam-gene:861
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_provenance
{
dgn-np:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_assertion
dcterms:description
"[To understand the cytogenetic mechanisms responsible for multiple RUNX1 gene copy numbers in hematologic malignancies, we analyzed the chromosomal and molecular cytogenetic findings in bone marrow or peripheral blood samples of individuals who were diagnosed with acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), or acute lymphoblastic leukemia (ALL).]. 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:19167608
;
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:NP238844.RA4xbrUiuchrZBMUVCEiV3BE7uN4ql_4veDJyy7pPB-H4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}