@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM
> .
@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:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_head
{
this:
np:hasAssertion
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_assertion
;
np:hasProvenance
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_provenance
;
np:hasPublicationInfo
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_assertion
a
np:Assertion
.
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_provenance
a
np:Provenance
.
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNb25d5eff6c16bd6110c1bc71d9f2993b
sio:SIO_000628
miriam-gene:3077
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_provenance
{
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_assertion
dcterms:description
"[Although each of these variants alone had relatively little effect on iron status, the combination of either HFE C282Y and HFE H63D or of HFE C282Y and transferrin C2 markedly raised transferrin saturation in those without dementia, but had little effect in those with mature Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:17047092
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP17801.RAtcVlWmHh-7iRh5gtnIVEQMCfgCfnvq_otTBb1dvyZYM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:06+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" .
}