@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg
> .
@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:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_head
{
this:
np:hasAssertion
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_assertion
;
np:hasProvenance
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_provenance
;
np:hasPublicationInfo
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_assertion
a
np:Assertion
.
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_provenance
a
np:Provenance
.
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_assertion
{
miriam-gene:23266
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN599cb4e084d0f8b8a8d932811a02af6a
sio:SIO_000628
miriam-gene:23266
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_provenance
{
dgn-np:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_assertion
dcterms:description
"[Interestingly, the frequencies of 194Trp and 399Gln genotypes were higher in colorectal cancer cases under age 40 than in corresponding controls, and an association between both polymorphisms and early age of disease onset was observed (OR=3.33, 95% CL 0.48-35.90, and P=0.16 for 194Trp and OR=11.90, 95% CL 2.30-51.50, and P=0.0003 for 399Gln).]. 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:10974409
;
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:NP154321.RAY6nXqUk8NWF3V6FO_IhdwE24v5B90MzPF1bwZtMRXCg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}