@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc
> .
@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:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_head
{
this:
np:hasAssertion
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_assertion
;
np:hasProvenance
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_provenance
;
np:hasPublicationInfo
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_assertion
a
np:Assertion
.
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_provenance
a
np:Provenance
.
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGN1d850bc0532d26f90d1acfaf618bb996
sio:SIO_000628
miriam-gene:2944
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_provenance
{
dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_assertion
dcterms:description
"[We examined the prevalence of GSTM1 and GSTT1 gene deletions, and two GSTP1 polymorphisms in 772 cases with advanced colorectal adenomas (>1 cm, villous elements or high-grade dysplasia) of the distal colon (descending or sigmoid colon or rectum) and 777 sigmoidoscopy negative controls enrolled in the screening arm of the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.]. 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:16030123
;
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:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:14+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" .
}