@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8
> .
@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:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_head
{
this:
np:hasAssertion
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_assertion
;
np:hasProvenance
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_provenance
;
np:hasPublicationInfo
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_assertion
a
np:Assertion
.
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_provenance
a
np:Provenance
.
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_assertion
{
miriam-gene:933
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN873ea2da350dcf54f9d3caf7fb454382
sio:SIO_000628
miriam-gene:933
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_provenance
{
dgn-np:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_assertion
dcterms:description
"[We have studied immunological features of 200 cases of acute leukemia (109 acute myelogenous leukemia, AML, and 91 acute lymphoblastic leukemia, ALL, according to FAB criteria), including 17 (8.5%) classified as biphenotypic by a scoring system based on the number and specificity of unexpected lineage antigens and which gives more weight to cytoplasmic markers such as myeloperoxidase, CD3, and CD22, and less to other membrane markers.]. 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:8501986
;
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:NP279890.RAcHgw21hcCCODMEWabKUin5QTgc68aycdoKQ02r6tFp8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}