@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q
> .
@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:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_head
{
this:
np:hasAssertion
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_assertion
;
np:hasProvenance
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_assertion
a
np:Assertion
.
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_provenance
a
np:Provenance
.
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_assertion
{
miriam-gene:1869
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNb94ce8cf029a77bce267194492ca1b8d
sio:SIO_000628
miriam-gene:1869
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_provenance
{
dgn-np:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_assertion
dcterms:description
"[Although deletions or structural rearrangements of E2F1 were not detected in 14 primary acute leukemia or myelodysplasia samples with structural abnormalities of chromosome 20q11, the gene was amplified and overexpressed in HEL erythroleukemia cells and translocated to other chromosomes in several established human leukemia cell lines.]. 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:7774910
;
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:NP295554.RA7R98uvS94V_FkZzPgKDRBbfunx_imb983Z29lAtAZ_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}