@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow
> .
@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:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_head
{
this:
np:hasAssertion
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_assertion
;
np:hasProvenance
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_provenance
;
np:hasPublicationInfo
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_assertion
a
np:Assertion
.
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_provenance
a
np:Provenance
.
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_assertion
{
miriam-gene:3612
a
ncit:C16612
.
lld:C0349640
a
ncit:C7057
.
dgn-gda:DGN5564261431268176deeba44a02ade6d2
sio:SIO_000628
miriam-gene:3612
,
lld:C0349640
;
a
sio:SIO_001121
.
}
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_provenance
{
dgn-np:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_assertion
dcterms:description
"[Using four criteria (monocytosis, percentage of IMP, basophilia, and percentage of erythroblasts in BM), patients could be divided into typical and atypical CML and this classification correlated well with molecular findings.]. 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:2070054
;
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:NP250003.RAQkf0JSH4nsH1gdkQxhna550IvWm5w_cQ7W83zjzOlow130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}