@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c
> .
@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:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_head
{
this:
np:hasAssertion
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_assertion
;
np:hasProvenance
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_provenance
;
np:hasPublicationInfo
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_assertion
a
np:Assertion
.
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_provenance
a
np:Provenance
.
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGNca7eaf63b263fe02d1b3a28297c429cd
sio:SIO_000628
miriam-gene:348
,
lld:C0282193
;
a
sio:SIO_001121
.
}
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_provenance
{
dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_assertion
dcterms:description
"[In this pilot study, common variants of the apolipoprotein E (APOE) and HFE genes resulting in the iron overload disorder of hereditary hemochromatosis (C282Y, H63D and S65C) were evaluated as factors in sporadic AD in an Ontario sample in which folic acid fortification has been mandatory since 1998.]. 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:18525129
;
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:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}