@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q
> .
@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:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_head
{
this:
np:hasAssertion
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_assertion
;
np:hasProvenance
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_assertion
a
np:Assertion
.
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_provenance
a
np:Provenance
.
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNe869e6f8464395f06748aef438ef86dd
sio:SIO_000628
miriam-gene:1543
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_provenance
{
dgn-np:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_assertion
dcterms:description
"[In this retrospective analysis, we examined key candidate gene polymorphisms in CYP1A1, EPHX1, GSTT1, GSTM1, and GSTP1 as modifiers of age at onset of colorectal cancer among 257 individuals with Lynch syndrome.]. 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:18768509
;
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:NP492750.RA2JN7LMUod-E3foLYFYdeEgDJMMbdjT9uGbPN8qrrg7Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}