@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA
> .
@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:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_head
{
this:
np:hasAssertion
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_assertion
;
np:hasProvenance
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_provenance
;
np:hasPublicationInfo
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_assertion
a
np:Assertion
.
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_provenance
a
np:Provenance
.
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C1879321
a
ncit:C7057
.
dgn-gda:DGN25e3e5a087f18ebf0f3007014de9e2aa
sio:SIO_000628
miriam-gene:2187
,
lld:C1879321
;
a
sio:SIO_001121
.
}
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_provenance
{
dgn-np:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_assertion
dcterms:description
"[Certain cytogenetic changes were closely associated with French-American-British (FAB) morphology, age, and outcome: t(8;21) (closely associated with FAB M2), t(15;17) (associated with FAB M3), and abn 16q22 (associated with FAB M4EOS) tended to occur in younger patients and were associated with favorable outcomes in terms of both CR rate and long-term disease-free survival.]. 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:2910364
;
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:NP641727.RAPflqfPQ0c3lqecNAXbvyeiU_cPM6iWwkDKPvPU-MjLA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:27+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" .
}