@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw
> .
@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:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_head
{
this:
np:hasAssertion
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_assertion
;
np:hasProvenance
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_provenance
;
np:hasPublicationInfo
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_assertion
a
np:Assertion
.
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_provenance
a
np:Provenance
.
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_assertion
{
miriam-gene:3240
a
ncit:C16612
.
lld:C0003969
a
ncit:C7057
.
dgn-gda:DGNc63f9c863be62b964e8cc1ed4abdf218
sio:SIO_000628
miriam-gene:3240
,
lld:C0003969
;
a
sio:SIO_001122
.
}
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_provenance
{
dgn-np:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_assertion
dcterms:description
"[Individuals with the Hp2-2 genotype had an increased risk of deficiency if they did not meet the Recommended Dietary Allowance for vitamin C, whereas carriers of the Hp1 allele did not. The findings suggest that the greater antioxidant capacity of Hp1 might spare serum ascorbic acid.]. 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:20926521
;
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:NP86523.RA5cFee7_VVjvkiEIZ9uEnv_o8srMDEMmN4itfK6xifVw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}