@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0
> .
@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:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_head
{
this:
np:hasAssertion
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_assertion
;
np:hasProvenance
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_provenance
;
np:hasPublicationInfo
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_assertion
a
np:Assertion
.
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_provenance
a
np:Provenance
.
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0035528
a
ncit:C7057
.
dgn-gda:DGN1163ae152bffff4395e65dad9c85b42a
sio:SIO_000628
miriam-gene:4524
,
lld:C0035528
;
a
sio:SIO_001121
.
}
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_provenance
{
dgn-np:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_assertion
dcterms:description
"[We tested the hypothesis that methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism, folic acid deficiency and riboflavin deficiency, independently or interactively, are important determinants of genomic stability, cell death, cell proliferation and homocysteine (Hcy) concentration in 9-d human lymphocyte cultures.]. 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:14704292
;
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:NP459597.RAmdOjw3yn2WDVgnToI-5CfvFXF2gwk4LJDg6fSYhhud0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:33+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" .
}