@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP591207.RAi-d51nGJ0rT1Al7nOI0o06oe-L1L9-QkEgVK1Bko7nA
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP591207.RAi-d51nGJ0rT1Al7nOI0o06oe-L1L9-QkEgVK1Bko7nA130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
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;
a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP591207.RAi-d51nGJ0rT1Al7nOI0o06oe-L1L9-QkEgVK1Bko7nA130_provenance
a
np:Provenance
.
dgn-np:NP591207.RAi-d51nGJ0rT1Al7nOI0o06oe-L1L9-QkEgVK1Bko7nA130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP591207.RAi-d51nGJ0rT1Al7nOI0o06oe-L1L9-QkEgVK1Bko7nA130_assertion
{
miriam-gene:57817
a
ncit:C16612
.
lld:C0162316
a
ncit:C7057
.
dgn-gda:DGN5a576eecd112d6e816301c179380b039
sio:SIO_000628
miriam-gene:57817
,
lld:C0162316
;
a
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.
}
dgn-np:NP591207.RAi-d51nGJ0rT1Al7nOI0o06oe-L1L9-QkEgVK1Bko7nA130_provenance
{
dgn-np:NP591207.RAi-d51nGJ0rT1Al7nOI0o06oe-L1L9-QkEgVK1Bko7nA130_assertion
dcterms:description
"[In the present study, we examined gene expression of duodenal iron transport molecules and hepcidin in patients with hereditary hemochromatosis (HHC) (treated and untreated), involving various genotypes (genotypes which represent risk for HHC were examined), and in patients with iron deficiency anaemia (IDA).]. 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:21973163
;
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:NP591207.RAi-d51nGJ0rT1Al7nOI0o06oe-L1L9-QkEgVK1Bko7nA130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
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pav:version
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}