@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A
> .
@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:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_head
{
this:
np:hasAssertion
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_assertion
;
np:hasProvenance
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_provenance
;
np:hasPublicationInfo
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_assertion
a
np:Assertion
.
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_provenance
a
np:Provenance
.
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_assertion
{
miriam-gene:7015
a
ncit:C16612
.
lld:C0265219
a
ncit:C7057
.
dgn-gda:DGNfd2ae40593d464b1141acaca418066fb
sio:SIO_000628
miriam-gene:7015
,
lld:C0265219
;
a
sio:SIO_001121
.
}
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_provenance
{
dgn-np:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_assertion
dcterms:description
"[We hypothesize that mad1 increase can contribute to reduce the hTERT expression in the early stage of disease and we suggest that hTERT expression and telomerase activity, whether confirmed in larger series of cases could support other parameters in the diagnosis and stadiation of MDS.]. 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:19270495
;
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:NP155442.RAPUqmSxroPCosigavkpi3QVJQjTm8V5SMITHoWxjC2-A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}