@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c
> .
@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:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_head
{
this:
np:hasAssertion
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion
;
np:hasProvenance
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance
;
np:hasPublicationInfo
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion
a
np:Assertion
.
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance
a
np:Provenance
.
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion
{
miriam-gene:1612
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN1495f8bf5ecfa397d0de3acdc0da4531
sio:SIO_000628
miriam-gene:1612
,
lld:C0023434
;
a
sio:SIO_001122
.
}
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_provenance
{
dgn-np:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_assertion
dcterms:description
"[Study shows that loss or reduced expression of DAPK1 underlies cases of heritable predisposition to chronic lymphocytic leukemia (CLL) and epigenetic silencing of DAPK1 by promoter methylation occurs in almost all sporadic CLL cases.]. 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:17540169
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP133673.RAf8gWnHkcvn9erioU55p3HiFI4-tY-Xb7nhSBUm5j59c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:09+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: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" .
}