@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko
> .
@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:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_head
{
this:
np:hasAssertion
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_assertion
;
np:hasProvenance
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_provenance
;
np:hasPublicationInfo
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_assertion
a
np:Assertion
.
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_provenance
a
np:Provenance
.
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0080178
a
ncit:C7057
.
dgn-gda:DGNa10516c231bdcc238b891942304b8ff0
sio:SIO_000628
miriam-gene:4524
,
lld:C0080178
;
a
sio:SIO_001122
.
}
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_provenance
{
dgn-np:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_assertion
dcterms:description
"[Based upon our observations, it is suggested that the association between the infant MTHFR homozygous variant genotype and spina bifida risk may be conditional upon both lesion level and maternal vitamin use.]. 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:12797455
;
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:NP69472.RAvrKcgqFOvDQVjQIHZCsWeh2fcp2V3oWNNvGVVe9_nko130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:33+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" .
}