@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ
> .
@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:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_head
{
this:
np:hasAssertion
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_assertion
;
np:hasProvenance
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_assertion
a
np:Assertion
.
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_provenance
a
np:Provenance
.
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_assertion
{
miriam-gene:217
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNb8cbede849bfb9c80acb234d33fdd431
sio:SIO_000628
miriam-gene:217
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_provenance
{
dgn-np:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_assertion
dcterms:description
"[A nested case-control study (1269 cases matched to 2107 controls by sex, age, study centre and date of blood collection) was conducted within the European Prospective Investigation into Cancer and Nutrition (EPIC) to evaluate the impact of rs1229984 (ADH1B), rs1573496 (ADH7) and rs441 (ALDH2) polymorphisms on CRC risk.]. 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:23149980
;
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:NP525916.RAxmU5tZcP9E6tZWXuzNKzS1485ckCmi56mdvLAyRxmwQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}