@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE
> .
@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:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_head
{
this:
np:hasAssertion
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_assertion
;
np:hasProvenance
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_provenance
;
np:hasPublicationInfo
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_assertion
a
np:Assertion
.
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_provenance
a
np:Provenance
.
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_assertion
{
miriam-gene:688
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNb5e2890ec0c1deeba077de1cfef619c8
sio:SIO_000628
miriam-gene:688
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_provenance
{
dgn-np:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_assertion
dcterms:description
"[Each of the cases with hemizygous deletion also exhibited loss of KLF5 expression, suggesting that loss of expression can result from chromosomal deletion, and that KLF5 may undergo haploinsufficiency during carcinogenesis.]. 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:12242654
;
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:NP691901.RAajH7wAUFv5wqwq3SF8BGiRccmGmA_nT9ccuFbhVIwxE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}