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http://rdf.disgenet.org/nanopublications.trig#NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
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;
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a
np:Nanopublication
.
dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_assertion
a
np:Assertion
.
dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_provenance
a
np:Provenance
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dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_publicationInfo
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{
miriam-gene:4524
a
ncit:C16612
.
lld:C0155626
a
ncit:C7057
.
dgn-gda:DGNf48cad120b90b2b63fa5d58767dd1c92
sio:SIO_000628
miriam-gene:4524
,
lld:C0155626
;
a
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.
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dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_provenance
{
dgn-np:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_assertion
dcterms:description
"[We have examined the prevalence of the C677T and A1298C single nucleotide polymorphisms (SNPs) in the methylenetetrahydrofolate reductase (MTHFR) gene in healthy Tamilians and in patients with acute myocardial infarction and related this polymorphism to plasma homocysteine concentrations, serum folate, serum cobalamin and riboflavin status.]. 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:17412321
;
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:NP238912.RALeh5NJDbOISL-rFrHABpXKyUE5HSMkxncRS93Vca0dQ130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
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