@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k
> .
@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:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_head
{
this:
np:hasAssertion
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_assertion
;
np:hasProvenance
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_assertion
a
np:Assertion
.
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_provenance
a
np:Provenance
.
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_assertion
{
miriam-gene:5063
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNa59642160a95557d9e5911a3a2373be3
sio:SIO_000628
miriam-gene:5063
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_provenance
{
dgn-np:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_assertion
dcterms:description
"[Polymorphic variants of p53 at codon 72, and CDKN1A at codon 31, have been found to be associated with cancer susceptibility, but few studies have investigated their effect on endometriosis risk.]. 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:22199295
;
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:NP508511.RAxtXdWxNRT9IxE4YBh5LV7tqWyQsCpUYUrCRWchWIo9k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}