@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow
> .
@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:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_head
{
this:
np:hasAssertion
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_assertion
;
np:hasProvenance
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_provenance
;
np:hasPublicationInfo
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_assertion
a
np:Assertion
.
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_provenance
a
np:Provenance
.
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_assertion
{
miriam-gene:4297
a
ncit:C16612
.
lld:C0033027
a
ncit:C7057
.
dgn-gda:DGNd527813840ddb7926d2b1ac18b837c4f
sio:SIO_000628
miriam-gene:4297
,
lld:C0033027
;
a
sio:SIO_001121
.
}
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_provenance
{
dgn-np:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_assertion
dcterms:description
"[Translocations and other rearrangements of the MLL gene at chromosome band 11q23 are biologically and clinically important molecular abnormalities in infant acute leukemias, leukemias associated with chemotherapeutic topoisomerase II poisons and, less often, acute leukemias in adults or myelodysplastic syndrome.]. 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:19277575
;
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:NP583303.RAtGI2KVQuuLqYP7SSyC7_NM9701ZujIXK5cSbfn-_Cow130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}