@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk
> .
@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:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_head
{
this:
np:hasAssertion
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_assertion
;
np:hasProvenance
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_provenance
;
np:hasPublicationInfo
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_assertion
a
np:Assertion
.
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_provenance
a
np:Provenance
.
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_assertion
{
miriam-gene:29107
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN9376ecf76226821d85003487fbb877e1
sio:SIO_000628
miriam-gene:29107
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_provenance
{
dgn-np:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_assertion
dcterms:description
"[The t(7;11)(p15;p15) translocation is an uncommon balanced aberration which has been found predominantly in Orientals, frequently presenting as de novo acute myeloid leukemia (AML) and occasionally as chronic myeloid leukemia in blastic crisis.]. 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:9112426
;
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:NP573433.RAeQSbBG-rIWT_sJl2XdgMUWLXodPfhvUYx9X_cb8Ywdk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}