@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y
> .
@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:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_head
{
this:
np:hasAssertion
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_assertion
;
np:hasProvenance
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_assertion
a
np:Assertion
.
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_provenance
a
np:Provenance
.
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0699791
a
ncit:C7057
.
dgn-gda:DGN5fb55756fd7d6056a8ba99fa38205152
sio:SIO_000628
miriam-gene:1588
,
lld:C0699791
;
a
sio:SIO_001121
.
}
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_provenance
{
dgn-np:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_assertion
dcterms:description
"[Of the 108 SNPs in steroid hormone biosynthesis pathway related genes and PGR analyzed in the discovery phase, 23 SNPs in PGR in the recessive model and 10 SNPs in CYP19A1 in the recessive or additive models were significantly associated with increased gastric cancer risk (p<0.05).]. 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:23110082
;
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:NP684612.RAVFIOX145hvdiz4p4h0-bC4vGHGcaDs4nC_VBWUelT3Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}