@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI
> .
@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/v3.0.0/void/
> .
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_head
{
this:
np:hasAssertion
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_assertion
;
np:hasProvenance
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_provenance
;
np:hasPublicationInfo
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_assertion
a
np:Assertion
.
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_provenance
a
np:Provenance
.
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_assertion
{
miriam-gene:1874
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGNf51dbc0031a81234b28cf9a88f74d8a6
sio:SIO_000628
miriam-gene:1874
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_provenance
{
dgn-np:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_assertion
dcterms:description
"[These results suggest that mutations of the E2F4 gene, presumably caused by an abnormality of one of the DNA repair genes, may play an important role in development of ATL and childhood ALL.]. 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:10666234
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP363645.RACCWTNuHhWV_3HUp8e9NZqeqA1O01hZ2FjY_QtQXTbcI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:09+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}