@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ
> .
@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:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_head
{
this:
np:hasAssertion
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_assertion
;
np:hasProvenance
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_assertion
a
np:Assertion
.
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_provenance
a
np:Provenance
.
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0007103
a
ncit:C7057
.
dgn-gda:DGNba31e437fd2498eb81af024b2b5c47d3
sio:SIO_000628
miriam-gene:7157
,
lld:C0007103
;
a
sio:SIO_001121
.
}
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_provenance
{
dgn-np:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_assertion
dcterms: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 factors in Caucasian women.]. 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: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:NP270299.RAA2CK4rx5rIuUFv8bm57x6HVGd615yWXg09Mjk3DeAcQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:31+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: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" .
}