@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs
> .
@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:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_head
{
this:
np:hasAssertion
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_assertion
;
np:hasProvenance
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_provenance
;
np:hasPublicationInfo
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_assertion
a
np:Assertion
.
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_provenance
a
np:Provenance
.
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0700095
a
ncit:C7057
.
dgn-gda:DGN4fe2466aff24b0a238c6c4519568429c
sio:SIO_000628
miriam-gene:4193
,
lld:C0700095
;
a
sio:SIO_001121
.
}
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_provenance
{
dgn-np:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_assertion
dcterms:description
"[A cohort of 497 NB children, enrolled in the Italian Neuroblastoma Registry between January 1985 and December 2005 and previously investigated for the prognostic role of MDM2 SNP309, was considered for this study.]. 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:20232446
;
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:NP188957.RAgBTs_c_C92LFN_Z_gNVspcfwd11C8k2RYTCYyqkcZOs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}