@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8
> .
@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:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_head
{
this:
np:hasAssertion
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_assertion
;
np:hasProvenance
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_provenance
;
np:hasPublicationInfo
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_assertion
a
np:Assertion
.
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_provenance
a
np:Provenance
.
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGNeb8353c3cf2ff2d47671aaa4b29e1212
sio:SIO_000628
miriam-gene:1029
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_provenance
{
dgn-np:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_assertion
dcterms:description
"[Our striking findings were that the risk increased 5.16, 8.28 and 4.10-fold, respectively, for NSCLC with promoter hypermethylation of the p16, DAPK or RAR beta gene in smokers with CYP1A1 variants, and the higher risk significantly increased in smokers with null GSTM1 and the OR was 17.84 for NSCLC with p16 promoter hypermethylation, 17.41 for DAPK, and 8.18 for RAR beta in smokers with null GSTM1 compared with controls (all p < 0.01).]. 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:20704749
;
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:NP196757.RAY5jCQhnyjWpbvsjZcu2BIYcue-OqtAtbxnykfXFvOv8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}