@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek
> .
@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:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_head
{
this:
np:hasAssertion
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_assertion
;
np:hasProvenance
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_provenance
;
np:hasPublicationInfo
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_assertion
a
np:Assertion
.
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_provenance
a
np:Provenance
.
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C0003969
a
ncit:C7057
.
dgn-gda:DGN0937c89fdafbcef30880f146e98692fd
sio:SIO_000628
miriam-gene:133482
,
lld:C0003969
;
a
sio:SIO_001121
.
}
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_provenance
{
dgn-np:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_assertion
dcterms:description
"[Individuals with GST null genotypes had an increased risk of deficiency if they did not meet the Recommended Dietary Allowance for vitamin C, which suggests that the GST enzymes protect against serum ascorbic acid deficiency when dietary vitamin C is insufficient.]. 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:19710200
;
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:NP491840.RA4zuJXopyFt14XzrADyTwKeni6-FungPXUV9-NmyPiek130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}