@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk
> .
@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:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_head
{
this:
np:hasAssertion
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_assertion
;
np:hasProvenance
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_provenance
;
np:hasPublicationInfo
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_assertion
a
np:Assertion
.
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_provenance
a
np:Provenance
.
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_assertion
{
miriam-gene:7321
a
ncit:C16612
.
lld:C0018995
a
ncit:C7057
.
dgn-gda:DGNd9a4fa74751ee5e36b9077aa43cb53d0
sio:SIO_000628
miriam-gene:7321
,
lld:C0018995
;
a
sio:SIO_001121
.
}
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_provenance
{
dgn-np:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_assertion
dcterms:description
"[Recent studies have demonstrated that although SFT expression is reciprocally regulated in response to cellular iron levels, it is aberrantly upregulated in the liver of hemochromatosis patients, indicating that enhanced SFT expression contributes to the etiology of this 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:9918797
;
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:NP283628.RAbqkf2F7oRLTw1L7qTUW8MBGRAbNEL_dvALYVYuf8EIk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+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" .
}