@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc
> .
@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 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:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_head
{
this:
np:hasAssertion
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_assertion
;
np:hasProvenance
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_provenance
;
np:hasPublicationInfo
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_assertion
a
np:Assertion
.
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_provenance
a
np:Provenance
.
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0014170
a
ncit:C7057
.
dgn-gda:DGN28203fa1f9a55adb173d5766cea0b964
sio:SIO_000628
miriam-gene:7157
,
lld:C0014170
;
a
sio:SIO_001122
.
}
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_provenance
{
dgn-np:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_assertion
dc:description
"[Our data did not demonstrate any significant difference in the prevalence of the p53 Arg72Pro genotype between patients and controls, providing evidence that this polymorphism is only weakly associated with the risk of endometrial cancer and prognostic fa]. 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:19209008
;
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:NP80278.RAfYeRTegZZrziT4yZgpDrWGit6yFTIGWbp3fmjrxbcCc130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}