@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY
> .
@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:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_head
{
this:
np:hasAssertion
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_assertion
;
np:hasProvenance
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_provenance
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np:hasPublicationInfo
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_assertion
a
np:Assertion
.
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_provenance
a
np:Provenance
.
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN35b02ce2b65ca6d1dda01793d498d032
sio:SIO_000628
miriam-gene:7157
,
lld:C1961102
;
a
sio:SIO_001122
.
}
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_provenance
{
dgn-np:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_assertion
dcterms:description
"[To investigate its relevance in childhood acute lymphoblastic leukemia (ALL) susceptibility, we genotyped 114 cases and 414 newborn controls from Wales (UK) for polymorphisms in TP53 (R72P), its negative regulator MDM2 (single-nucleotide polymorphism SNP309, rs2279744), and selected HLA complex genes whose products interact with TP53.]. 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:19837266
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP80316.RAp2dHwPFdceq1VPYkVQ4VHGlbeSwxpNNoaZ5rTgNt2mY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:39+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" .
}