@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY
> .
@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:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_head
{
this:
np:hasAssertion
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_assertion
;
np:hasProvenance
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_provenance
;
np:hasPublicationInfo
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_assertion
a
np:Assertion
.
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_provenance
a
np:Provenance
.
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C1333762
a
ncit:C7057
.
dgn-gda:DGN25b9d91a17f79f5096a745411114db61
sio:SIO_000628
miriam-gene:4524
,
lld:C1333762
;
a
sio:SIO_001121
.
}
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_provenance
{
dgn-np:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_assertion
dcterms:description
"[In most studies, the MTHFR 677TT (variant) genotype, which is associated with reduced enzyme activity, was associated with an increased risk of esophageal squamous cell carcinoma, gastric cardia adenocarcinoma, noncardia gastric cancer, gastric cancer (all subsites), and pancreatic cancer; all but one of 22 odds ratios were >1, of which 13 estimates were statistically significant.]. 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:17030196
;
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:NP557670.RAOgTYUyShovvB8UXYQ7Xe9jrPA9ARhhv39ZMniM9-AbY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}