@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_assertion
a
np:Assertion
.
dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_provenance
a
np:Provenance
.
dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_publicationInfo
a
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.
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dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_assertion
{
miriam-gene:1559
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN51e05d28af46ec842d2d9be5691a4c14
sio:SIO_000628
miriam-gene:1559
,
lld:C0009402
;
a
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.
}
dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_provenance
{
dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_assertion
dcterms:description
"[We investigated whether 35 functionally relevant polymorphisms within CYP2C9 and UGT genes were associated with colorectal cancer risk or modified the protective effect of NSAIDs on colorectal cancer susceptibility, using 1,584 colorectal cancer cases and 2,516 unaffected sibling controls from the Colon Cancer Family Registry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:24677636
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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 .
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dgn-np:NP341890.RAgN7M6DKqhm9dJPHLj8qq1nicOWrXXBFMVFrG5eh3arw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:57+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
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