@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ
> .
@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:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_head
{
this:
np:hasAssertion
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_assertion
;
np:hasProvenance
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_assertion
a
np:Assertion
.
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_provenance
a
np:Provenance
.
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGNe22e29b6d10535ce2be553b470390c8d
sio:SIO_000628
miriam-gene:472
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_provenance
{
dgn-np:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_assertion
dcterms:description
"[In a Swedish population-based case-control study including 705 cases and 1565 controls, we examined common variation in the ATM, CHEK2 and ERBB2 genes in relation to endometrial cancer risk overall, restricted to tumours of certain characteristics or stratified by various endometrial cancer risk factors.]. 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:17164260
;
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:NP762792.RAD9vjAEedW2C6t1e_tKzhO_IprX5YngSX-6jQZR9U8RQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}