@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg
> .
@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:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_head
{
this:
np:hasAssertion
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_assertion
;
np:hasProvenance
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_provenance
;
np:hasPublicationInfo
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_assertion
a
np:Assertion
.
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_provenance
a
np:Provenance
.
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_assertion
{
miriam-gene:1386
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGNfdb9caadfacbebebbd8fa185f675f7f1
sio:SIO_000628
miriam-gene:1386
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_provenance
{
dgn-np:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_assertion
dcterms:description
"[Significance analysis of microarray (SAM) identified 27 differentially expressed genes between these two subgroups with significant overexpression of ATF5 and underexpression of CDC16, PCDH8, SLAM, MNDA and ATF2 in CLL patients with poor outcome.]. 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:17786276
;
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:NP668597.RAUsblLldyUm7ah_AtcY8skzGKCrzhJDldKzwvpb75chg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}