@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY
> .
@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:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_head
{
this:
np:hasAssertion
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_assertion
;
np:hasProvenance
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_assertion
a
np:Assertion
.
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_provenance
a
np:Provenance
.
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNb2ac829c321cea39367cc20b4ec277dd
sio:SIO_000628
miriam-gene:7157
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_provenance
{
dgn-np:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_assertion
dcterms:description
"[Increased incidence of p53 gene aberrations or chromosome 17p monosomy resulting from an isochromosome 17q [i(17q)] has been observed with transition of chronic myelogenous leukemia (CML) to myeloid blast crisis (BC), and in some patients with poor risk acute myeloid leukemia (AML) progressing from myelodysplastic syndrome (MDS).]. 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:8505851
;
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:NP273327.RAqExtx6yQz7p5mc6Kxf2dPHl_-J8RuclEWcWfJpHxvUY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}