@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18130_assertion
;
np:hasProvenance
dgn-np:NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18130_provenance
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np:hasPublicationInfo
dgn-np:NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18130_publicationInfo
;
a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18130_provenance
a
np:Provenance
.
dgn-np:NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:4524
a
ncit:C16612
.
lld:C0751955
a
ncit:C7057
.
dgn-gda:DGN076a86c5ac1d6919930879830037fc6f
sio:SIO_000628
miriam-gene:4524
,
lld:C0751955
;
a
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.
}
dgn-np:NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18130_provenance
{
dgn-np:NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18130_assertion
dcterms:description
"[To evaluate whether hyperhomocysteinemia is an independent risk factor for silent brain infarction (SBI), and to determine the relationship between homocysteine and folate in each type of methylenetetrahydrofolate reductase (MTHFR) polymorphism, in order to identify a way of reducing the risk for SBI.]. 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:14663048
;
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:NP571778.RARBEhD_z9tF55I2Zb4m4K1Yl6JK_BFxcPFw5XAu-JC18130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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