@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA
> .
@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:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_head
{
this:
np:hasAssertion
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_assertion
;
np:hasProvenance
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_provenance
;
np:hasPublicationInfo
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_assertion
a
np:Assertion
.
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_provenance
a
np:Provenance
.
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_assertion
{
miriam-gene:57817
a
ncit:C16612
.
lld:C0392514
a
ncit:C7057
.
dgn-gda:DGNacff0238566164eaaba8a27eb114fe09
sio:SIO_000628
miriam-gene:57817
,
lld:C0392514
;
a
sio:SIO_001121
.
}
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_provenance
{
dgn-np:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_assertion
dcterms:description
"[Knowledge of the regulation of hepcidin by inflammation, iron, erythropoiesis, and hypoxia will lead to an understanding of the pathogenesis of primary hemochromatosis, secondary iron overload, and anemia of inflammatory disease.]. 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:19400694
;
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:NP509658.RACeMvWC2Xf0j9BnfAbehm_DXoi_P-RtsRKkLyXTDw1SA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}