@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw
> .
@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:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_head
{
this:
np:hasAssertion
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_assertion
;
np:hasProvenance
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_provenance
;
np:hasPublicationInfo
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_assertion
a
np:Assertion
.
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_provenance
a
np:Provenance
.
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C0235956
a
ncit:C7057
.
dgn-gda:DGNe1122f2f4c3b33d1e0d0b2027e841be7
sio:SIO_000628
miriam-gene:2187
,
lld:C0235956
;
a
sio:SIO_001121
.
}
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_provenance
{
dgn-np:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_assertion
dcterms:description
"[We describe a 30-year-old acute myelomonocytic leukemia patient with abnormal bone marrow eosinophils (AML FAB subtype M4Eo) with extensive extramedullary involvement and, in the abscence of an aberration involving chromosome 16, clonal trisomy 21 in the leukemic blast cells.]. 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:8148422
;
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:NP779537.RAPRwFUXhKXCCzcUeKohtESEydJnr0YQkLGi4wNPCRMnw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}