@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_assertion
a
np:Assertion
.
dgn-np:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_provenance
a
np:Provenance
.
dgn-np:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0795864
a
ncit:C7057
.
dgn-gda:DGNeedf0fd6e14e12793fcbb2d55fd7db96
sio:SIO_000628
miriam-gene:7157
,
lld:C0795864
;
a
sio:SIO_001121
.
}
dgn-np:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_provenance
{
dgn-np:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_assertion
dcterms:description
"[Thus, our data suggest that there is no association between i(17q) and coding TP53 mutations, and that another tumor suppressor gene(s), located in proximity of the SMS common deletion region, or in a more distal location, is of pathogenetic importance in i(17q)-associated 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:10381517
;
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:NP285622.RAo99IFhoB19UWenLHNmg8ojuzttcarEjr_PffzAuQ0q8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:41+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
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pav:authoredBy
<
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> , <
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
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"v2.1.0" .
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