@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM
> .
@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:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_head
{
this:
np:hasAssertion
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_assertion
;
np:hasProvenance
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_provenance
;
np:hasPublicationInfo
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_assertion
a
np:Assertion
.
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_provenance
a
np:Provenance
.
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_assertion
{
miriam-gene:6776
a
ncit:C16612
.
lld:C0079731
a
ncit:C7057
.
dgn-gda:DGNb76a32c09d4f5af63d177c1fcd48f94e
sio:SIO_000628
miriam-gene:6776
,
lld:C0079731
;
a
sio:SIO_001121
.
}
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_provenance
{
dgn-np:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_assertion
dcterms:description
"[In contrast, STAT5(S711F) was found to cooperate with the loss of function of the p53 tumor suppressor gene to both accelerate disease onset and to skew the large tumor spectrum that normally characterize p53-deficient mice to strongly favor B-cell lymphoma/leukemia.]. 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:16532027
;
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:NP676330.RA4OMW8CzdtKXGyO1rs2oq99hsm9gVWLlbUhkk8zhbMWM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}