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http://rdf.disgenet.org/nanopublications.trig#NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_assertion
;
np:hasProvenance
dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_provenance
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np:hasPublicationInfo
dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_publicationInfo
;
a
np:Nanopublication
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dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_assertion
a
np:Assertion
.
dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_provenance
a
np:Provenance
.
dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_assertion
{
miriam-gene:4552
a
ncit:C16612
.
lld:C0080178
a
ncit:C7057
.
dgn-gda:DGNc02e4893076a1edf039ad0fdaf267665
sio:SIO_000628
miriam-gene:4552
,
lld:C0080178
;
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.
}
dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_provenance
{
dgn-np:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_assertion
dcterms:description
"[We evaluated the association of polymorphisms of three genes affecting vitamin B12-dependent remethylation of homocysteine, transcobalamin (TC), methionine synthase (MTR) and MTR reductase (MTRR), combined or not with methylenetetrahydrofolate reductase (MTHFR), with the risk of having neural tube defect in 40 children with spina bifida and 58 matched controls from South Italy.]. 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:12812837
;
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:NP268657.RAaalAOsjNlFZ7JQHzt97DqLw0QTe9jfyDWAyF5NQC_80130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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
;
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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