@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw
> .
@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:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_head
{
this:
np:hasAssertion
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_assertion
;
np:hasProvenance
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_provenance
;
np:hasPublicationInfo
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_assertion
a
np:Assertion
.
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_provenance
a
np:Provenance
.
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_assertion
{
miriam-gene:596
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN026e138dea57812406140cd6369de5b1
sio:SIO_000628
miriam-gene:596
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_provenance
{
dgn-np:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_assertion
dcterms:description
"[These data suggest that BCL2 is involved differently in different types (favorable versus unfavorable) of AML and that therapeutic strategies aimed at modulating BCL2 function may be more likely to work in patients with favorable cytogenetic abnormalities.]. 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:10430080
;
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:NP158548.RA10AHFjzYDCtbFmfqzVDYJxQPoNHkEgJaI50fFTCYtVw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:25+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" .
}