@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM
> .
@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:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_head
{
this:
np:hasAssertion
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_assertion
;
np:hasProvenance
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_provenance
;
np:hasPublicationInfo
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_assertion
a
np:Assertion
.
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_provenance
a
np:Provenance
.
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_assertion
{
miriam-gene:4548
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGNf282792e57f2d130a13afaf50e4db2aa
sio:SIO_000628
miriam-gene:4548
,
lld:C0013080
;
a
sio:SIO_001122
.
}
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_provenance
{
dgn-np:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_assertion
dcterms:description
"[The aim of the present study was to investigate the effect of polymorphisms C677T and A1298C in the methylenetetrahydrofolate reductase (MTHFR) gene, A2756G in methionine synthase reductase (MTR) gene and A80G in reduced folate carrier 1 (RFC1) gene, and plasma homocysteine (Hcy), on the maternal risk for Down syndrome (DS).]. 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:18273817
;
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:NP61576.RA7ogNJw3Fh5a-X0M-pxJALrclLAdIBqj4OM4g7tCVLQM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}