@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI
> .
@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:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_head
{
this:
np:hasAssertion
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_assertion
;
np:hasProvenance
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_provenance
;
np:hasPublicationInfo
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_assertion
a
np:Assertion
.
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_provenance
a
np:Provenance
.
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_assertion
{
miriam-gene:6470
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGNa2d12dabda59b4001145c12151ca9a4f
sio:SIO_000628
miriam-gene:6470
,
lld:C0024299
;
a
sio:SIO_001122
.
}
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_provenance
{
dgn-np:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_assertion
dcterms:description
"[Moreover, combined analysis of TS and SHMT1 polymorphisms revealed that the OR for lymphoma in patients with SHMT1 1420 CC and the TS 2R allele, which might be expected to provide the basis for the highest susceptibility, was 2.88 (95% CI, 1.26-6.58, p=0.013).]. 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:12604405
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP51755.RAWCTrfvRR5B99ZYy45FKODH_-6CbtWeeBkIXbSXktBQI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}