@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_head
{
this:
np:hasAssertion
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_assertion
;
np:hasProvenance
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_provenance
;
np:hasPublicationInfo
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_assertion
a
np:Assertion
.
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_provenance
a
np:Provenance
.
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_assertion
{
miriam-gene:613
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGNcb2479da5d3c2724abffdbe5d9d612c3
sio:SIO_000628
miriam-gene:613
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_provenance
{
dgn-np:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_assertion
dcterms:description
"[Although the association between inv(9) variation and CML is still controversial, we believe that hematologists should consider the role of constitutional inv(9) variation in CML patients to avoid overlooking the impaired engraftment potential of hematopoietic stem cells harboring inv(9).]. 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:20603579
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP823774.RAL3GUJ2CXeHxJ_nk6qSjCgBHBSUlPSB3hHDU788qQHHs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:58+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}