@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo
> .
@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:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_head
{
this:
np:hasAssertion
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_assertion
;
np:hasProvenance
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_provenance
;
np:hasPublicationInfo
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_assertion
a
np:Assertion
.
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_provenance
a
np:Provenance
.
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0279628
a
ncit:C7057
.
dgn-gda:DGN03d8e4447d3c398e0cd4168ac263f11b
sio:SIO_000628
miriam-gene:2944
,
lld:C0279628
;
a
sio:SIO_001121
.
}
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_provenance
{
dgn-np:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_assertion
dcterms:description
"[The strong statistical association between smoking and risk for EADC in individuals with the active allele of either GSTM1 or GSTT1 may have potential clinical application in endoscopic surveillance programs to identify individuals with BE at increased risk for progression to EADC.]. 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:17064856
;
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:NP938221.RApINmeNNbFaYUfhwMZEMtWKObThKVcJKtRjYKMbUnCgo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}