@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8
> .
@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:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_head
{
this:
np:hasAssertion
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_assertion
;
np:hasProvenance
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_provenance
;
np:hasPublicationInfo
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_assertion
a
np:Assertion
.
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_provenance
a
np:Provenance
.
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_assertion
{
miriam-gene:57817
a
ncit:C16612
.
lld:C0392514
a
ncit:C7057
.
dgn-gda:DGNac1819b30091d6a3bb8f96d40c5780f2
sio:SIO_000628
miriam-gene:57817
,
lld:C0392514
;
a
sio:SIO_001121
.
}
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_provenance
{
dgn-np:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_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:NP302073.RAjYC8Jhcu-zDMPOQuWv254oPspCZ_qkl-A0nq-87iCY8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:53+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" .
}