@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A
> .
@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:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_head
{
this:
np:hasAssertion
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_assertion
;
np:hasProvenance
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_provenance
;
np:hasPublicationInfo
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_assertion
a
np:Assertion
.
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_provenance
a
np:Provenance
.
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_assertion
{
miriam-gene:2122
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGN29ce7156e01e4e836ba02d05f47ed22d
sio:SIO_000628
miriam-gene:2122
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_provenance
{
dgn-np:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_assertion
dcterms:description
"[These results suggest that EVI1 overexpression was the major factor contributing to leukemogenesis, and the late appearance of the Ph chromosome is closely associated with the progression to an aggressive form of leukemia.]. 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:18206536
;
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:NP358776.RAGsVzkEJxsE9NnCiBjtYEuYZZlpavlczMOBtWXzOnF2A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}