@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64
> .
@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:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_head
{
this:
np:hasAssertion
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_assertion
;
np:hasProvenance
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_provenance
;
np:hasPublicationInfo
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_assertion
a
np:Assertion
.
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_provenance
a
np:Provenance
.
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0221013
a
ncit:C7057
.
dgn-gda:DGN2561dc58ea5abec4dbf6f5d199844e03
sio:SIO_000628
miriam-gene:26191
,
lld:C0221013
;
a
sio:SIO_001121
.
}
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_provenance
{
dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_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 ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:22051531
;
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:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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
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pav:authoredBy
<
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> , <
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> , <
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
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"v2.1.0" .
}