@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4
> .
@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:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_head
{
this:
np:hasAssertion
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_assertion
;
np:hasProvenance
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_provenance
;
np:hasPublicationInfo
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_assertion
a
np:Assertion
.
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_provenance
a
np:Provenance
.
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGNaefb914154dbf19955681942136bc8c2
sio:SIO_000628
miriam-gene:4524
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_provenance
{
dgn-np:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_assertion
dcterms:description
"[We have previously reported associations between lymphoma risk and germline polymorphisms in genes of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) and methionine synthase (MTR A2756G), finding the genotype other than the MTHFR 677CC/1298AA to confer a half-risk compared to the MTHFR 677CC/1298AA and a 3-fold higher risk with the MTR GG genotype than the AA/AG genotypes.]. 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:15551285
;
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:NP396360.RAGLfZHx8cyRbm4AYDluzx1tkwqOq1cdi_SxBLlp2DKN4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:56+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" .
}