@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_head
{
this:
np:hasAssertion
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_assertion
;
np:hasProvenance
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_provenance
;
np:hasPublicationInfo
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_assertion
a
np:Assertion
.
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_provenance
a
np:Provenance
.
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGN5ed388c2a6bf113c3d36d49209d17a7d
sio:SIO_000628
miriam-gene:348
,
lld:C0282193
;
a
sio:SIO_001122
.
}
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_provenance
{
dgn-np:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP245944.RAN5vn_cp7VTumoBZS_jDUx_QqPgwrMLlpc7J2hTULQYs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:00+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}