@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc
> .
@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:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_head
{
this:
np:hasAssertion
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_assertion
;
np:hasProvenance
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_provenance
;
np:hasPublicationInfo
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_assertion
a
np:Assertion
.
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_provenance
a
np:Provenance
.
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_assertion
{
miriam-gene:3811
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNbe5000907a1e05a80d5f46e9731fc6e9
sio:SIO_000628
miriam-gene:3811
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_provenance
{
dgn-np:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_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:NP853513.RAxwp0eGiuJ5fyN5I0umYfwnz3efVUjja5X94DUWllDsc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:42+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" .
}