@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw
> .
@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:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_head
{
this:
np:hasAssertion
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_assertion
;
np:hasProvenance
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_provenance
;
np:hasPublicationInfo
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_assertion
a
np:Assertion
.
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_provenance
a
np:Provenance
.
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGNb739f200fbb30808a8278034427a6d29
sio:SIO_000628
miriam-gene:2187
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_provenance
{
dgn-np:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_assertion
dcterms:description
"[Although the cause of leukaemia in Down syndrome (DS) remains unknown, potential candidate genes include the ones on chromosome 21, and in particular AML1, the rearrangement of which in the t(8,21) is associated with the French-American-British (FAB) classification M2 subtype of acute myeloid leukaemia (AML) in the general population and has been described in Down patients with AML-M2.]. 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:9177434
;
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:NP231320.RArg6l5qFWGxlzNq-vR1s_Dsj7Sa9QKqSY6WCpaAHKDpw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}