@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k
> .
@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:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_head
{
this:
np:hasAssertion
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_assertion
;
np:hasProvenance
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_provenance
;
np:hasPublicationInfo
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_assertion
a
np:Assertion
.
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_provenance
a
np:Provenance
.
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_assertion
{
miriam-gene:921
a
ncit:C16612
.
lld:C0024282
a
ncit:C7057
.
dgn-gda:DGN97cdb80e734812118c2c5804e37009b5
sio:SIO_000628
miriam-gene:921
,
lld:C0024282
;
a
sio:SIO_001121
.
}
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_provenance
{
dgn-np:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_assertion
dcterms:description
"[Apart from the diagnostic and prognostic value of laboratory abnormalities such as clonal lymphocytosis with CD5+CD19+CD23+ phenotype, reduced erythrocyte parameters, thrombocytopenia or bone marrow infiltration by the neoplastic clone as well as low percentage of Gumprecht's shadows, low apoptotic activity of peripheral blood lymphocytes, and increased percentage of CD38- and ZAP-70 ± cells markedly correlate with the stage of disease progression.]. 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:21626106
;
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:NP221737.RAxJXtI85-qoMXgDPKaYT_DeE1oh7slG3R-NcFcVD4P8k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}