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http://rdf.disgenet.org/nanopublications.trig#NP645221.RA5XP2oE00FUPj9_yexYH-uc2kgWgudjTlOauY8YCS7n8
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
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dgn-np:NP645221.RA5XP2oE00FUPj9_yexYH-uc2kgWgudjTlOauY8YCS7n8130_assertion
;
np:hasProvenance
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP645221.RA5XP2oE00FUPj9_yexYH-uc2kgWgudjTlOauY8YCS7n8130_provenance
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np:Provenance
.
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{
miriam-gene:5047
a
ncit:C16612
.
lld:C0221013
a
ncit:C7057
.
dgn-gda:DGNff120ba6f40024dcf2c384b569906fd0
sio:SIO_000628
miriam-gene:5047
,
lld:C0221013
;
a
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.
}
dgn-np:NP645221.RA5XP2oE00FUPj9_yexYH-uc2kgWgudjTlOauY8YCS7n8130_provenance
{
dgn-np:NP645221.RA5XP2oE00FUPj9_yexYH-uc2kgWgudjTlOauY8YCS7n8130_assertion
dcterms:description
"[Here, we assessed the potential association between the immunophenotype of MC and multilineage KIT mutation in the BM of SM patients through the investigation of the flow cytometric protein expression profile (PEP) of bone marrow mast cells (BMMC) from 70 control individuals and 206 SM patients, classified according to the WHO (World Health Organization), and the degree of involvement of BM hematopoiesis by the D816V KIT mutation; additionally, we developed a score-based class prediction algorithm for the detection of SM cases with multilineage mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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dgn-void:source_evidence_literature
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miriam-pubmed:22051531
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prov:wasGeneratedBy
eco:ECO_0000203
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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 .
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dgn-np:NP645221.RA5XP2oE00FUPj9_yexYH-uc2kgWgudjTlOauY8YCS7n8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:29+02:00"^^
xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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> , <
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pav:createdBy
<
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