@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4
> .
@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:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_head
{
this:
np:hasAssertion
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_assertion
;
np:hasProvenance
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_provenance
;
np:hasPublicationInfo
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_assertion
a
np:Assertion
.
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_provenance
a
np:Provenance
.
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_assertion
{
miriam-gene:10392
a
ncit:C16612
.
lld:C0014170
a
ncit:C7057
.
dgn-gda:DGN8e60d5bf05b7404fd679b15720eb1a50
sio:SIO_000628
miriam-gene:10392
,
lld:C0014170
;
a
sio:SIO_001122
.
}
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_provenance
{
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_assertion
dcterms:description
"[The variant C allele of rs5743836 causes greater TLR9 transcriptional activity compared to the T allele, therefore, higher TLR9 activity may be related to efficient removal of microbial pathogens within the endometrium. Clearly, the association of these TLR9 polymorphisms and endometrial cancer risk must be further examined in an independent population. The results point towards the importance of examining immune response in endometrial tumourigenesis to understand new pathways that may be implicated in disease.]. 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:20646321
;
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:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}