@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU
> .
@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:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_head
{
this:
np:hasAssertion
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_assertion
;
np:hasProvenance
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_provenance
;
np:hasPublicationInfo
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_assertion
a
np:Assertion
.
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_provenance
a
np:Provenance
.
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_assertion
{
miriam-gene:3952
a
ncit:C16612
.
lld:C0000786
a
ncit:C7057
.
dgn-gda:DGN2a4e44c64aca34d70864c4934310556c
sio:SIO_000628
miriam-gene:3952
,
lld:C0000786
;
a
sio:SIO_001121
.
}
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_provenance
{
dgn-np:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_assertion
dcterms:description
"[The present study revealed no significant differences between the genotypes or alleles of investigated polymorphism for endometrial cancer risk or its related traits (age of menarche, menopause, number of spontaneous abortions in personal history or waiting time till the onset of the disease) among the groups, thus indicating that the genetic variants of LEP-2548 G/A is not a relevant marker of endometrial cancer risk in this Czech population.]. 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:19886360
;
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:NP826432.RAHOch7rIey5A8pLbJog1fvTjBxNAHyL8wImtnm-CiMwU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:26+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" .
}