@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs
> .
@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:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_head
{
this:
np:hasAssertion
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_assertion
;
np:hasProvenance
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_provenance
;
np:hasPublicationInfo
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_assertion
a
np:Assertion
.
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_provenance
a
np:Provenance
.
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_assertion
{
miriam-gene:3439
a
ncit:C16612
.
lld:C0005699
a
ncit:C7057
.
dgn-gda:DGNbbdd17b0d9fa9b782cabeb7746ae8898
sio:SIO_000628
miriam-gene:3439
,
lld:C0005699
;
a
sio:SIO_001121
.
}
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_provenance
{
dgn-np:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_assertion
dcterms:description
"[We conclude that: (1) abnormal IgH fingerprints are found in a significant number of CP CML patients; (2) in this cohort the use of IFN was associated with normal CP CML IgH fingerprints, and (3) detection of abnormal IgH fingerprints may be highly predictive for the lineage of impending blast crisis.]. 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:10037027
;
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:NP574098.RA40WOY8X42V6RrAVC6Qtdfw-Wb1rPmrjHrKvPvQ1sCRs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}