@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o
> .
@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:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_head
{
this:
np:hasAssertion
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_assertion
;
np:hasProvenance
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_provenance
;
np:hasPublicationInfo
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_assertion
a
np:Assertion
.
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_provenance
a
np:Provenance
.
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN586cd2e4f9f4e710d6adde2a292782bc
sio:SIO_000628
miriam-gene:4709
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_provenance
{
dgn-np:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_assertion
dcterms:description
"[(1990) Cancer Res., 50, 5049-5054], the seven individuals with the highest observed frequencies of micronucleated erythrocytes all had exceptionally low values of plasma folate, red cell folate, or plasma B12, suggesting that folate and B12 status are the major determinants of the types of damage that lead to spontaneous micronucleus formation in erythrocytic cells.]. 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:9219587
;
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:NP439606.RA2C_BJqsRBp4ZSApgDR1u-ipoqGap7B-UO8gweMv-d6o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}