@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA
> .
@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:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_head
{
this:
np:hasAssertion
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_assertion
;
np:hasProvenance
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_provenance
;
np:hasPublicationInfo
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_assertion
a
np:Assertion
.
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_provenance
a
np:Provenance
.
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C0392514
a
ncit:C7057
.
dgn-gda:DGN2cf2f9c633462c49bc322c41ea2ce45c
sio:SIO_000628
miriam-gene:2056
,
lld:C0392514
;
a
sio:SIO_001121
.
}
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_provenance
{
dgn-np:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_assertion
dcterms:description
"[The purposes of this study were to evaluate the tolerance, efficacy and safety of isovolemic erythrocytapheresis (EA) in nonanemic patients with hereditary hemochromatosis (HH), and to assess the usefulness of recombinant human erythropoietin (rHuEPO) associated with EA to reduce treatment duration.]. 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:10971213
;
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:NP938478.RAIluFF0IdonZhhSS9wSG1jb8Th9BllO7oUbPQXjjFriA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}