@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w
> .
@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:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_head
{
this:
np:hasAssertion
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_assertion
;
np:hasProvenance
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_provenance
;
np:hasPublicationInfo
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_assertion
a
np:Assertion
.
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_provenance
a
np:Provenance
.
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_assertion
{
miriam-gene:48
a
ncit:C16612
.
lld:C0392514
a
ncit:C7057
.
dgn-gda:DGN06e7c8377bc08ea7f438d201a80b0f3a
sio:SIO_000628
miriam-gene:48
,
lld:C0392514
;
a
sio:SIO_001121
.
}
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_provenance
{
dgn-np:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_assertion
dcterms:description
"[As an inappropriate up-regulation of total IRP activity has been found in the duodenum and monocytes of patients with hereditary hemochromatosis (HH), we investigated the respective roles of IRP1 and IRP2 in these settings.]. 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:16503547
;
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:NP799914.RAEkR1r___YvhLKj30WzJa_imCcV78epUMkORuXlmrY5w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}