@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_head
{
this:
np:hasAssertion
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_assertion
;
np:hasProvenance
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_provenance
;
np:hasPublicationInfo
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_assertion
a
np:Assertion
.
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_provenance
a
np:Provenance
.
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNab9f107eac2294be54908e57d9d6d1be
sio:SIO_000628
miriam-gene:4193
,
lld:C0027651
;
a
sio:SIO_001122
.
}
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_provenance
{
dgn-np:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_assertion
dcterms:description
"[Studies of human genetic variants in the p53 tumor suppressor gene and MDM2 oncogene have shown that single nucleotide polymorphisms (SNP) can affect p53 signaling, confer cancer risk, and alter outcome, and also suggest that the pathway is under evolutionary selective pressure.]. 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:19773383
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP93329.RA0tuF6OAQOb_S1ge08eh0ktFJO6zMrkjsx9OiMvyP2HM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:31+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}