@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM
> .
@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:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_assertion
;
np:hasProvenance
dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_provenance
;
np:hasPublicationInfo
dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_assertion
a
np:Assertion
.
dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_provenance
a
np:Provenance
.
dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGNa7697788cd4096df18dd169c81a35679
sio:SIO_000628
miriam-gene:7157
,
lld:C0546837
;
a
sio:SIO_001122
.
}
dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_provenance
{
dgn-np:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_assertion
dcterms:description
"[This study aimed to evaluate the prognostic significance of two functional single nucleotide polymorphisms (SNP) in the p53 pathway (p53 Arg72Pro and MDM2 T309G) in patients with esophageal cancer, and to determine the importance of histologic subtype in the SNP-outcome relationships.]. 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:19383811
;
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:NP58721.RAdeR_dQWNQU4WpL1cICKdUUO4RWP2ixX4kxmbrBF6NwM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}